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    • 专利摘要:
    The present invention has no problem in production or handling, and is a basic organic compound that is catalytically active as a basic compound and soluble in an organic solvent, that is, phosphine sulfide represented by the general formula (1), and a method for producing the same The present invention relates to a method for producing phosphine sulfide represented by the general formula (1) by reacting 1 mol of thiophosphoranyl chloride with 3 mol of the phosphorane represented by the general formula (2). The present invention provides a method for efficiently preparing a poly (alkylene oxide) in the presence of the organic compound (phosphil sulfide), that is, having a partial structure of phosphine sulfide or phosphine sulfide and water and -OH or -NH-. Preparing a poly (alkylene oxide) by polymerizing an alkylene oxide in the presence of an active hydrogen compound selected from organic compounds; And a method for producing 1,2-dioxyethane derivatives from epoxy compounds, that is, 1,2-dioxy by reacting epoxy compounds with carboxylates, carboxylic anhydrides, carbonates or phenol compounds in the presence of phosphine sulfide, respectively. It relates to a method for producing an ethane derivative.
    公开号:KR20000011756A
    申请号:KR1019990028784
    申请日:1999-07-15
    公开日:2000-02-25
    发明作者:후나키카쯔히코；하라이사오；하야시타카오미；키요노신지；시바하라아쯔시；미즈타니카즈미；노보리타다히토；타카키우사지
    申请人:사토 아키오；미쯔이카가쿠 가부시기가이샤；
    IPC主号:
    专利说明:

    Phosphine sulfide, its manufacturing method and its use {A phosphine sulfide, a manufacturing process therefor and a use pretty}
    The present invention relates to novel useful phosphine sulfides represented by the general formula (1) and a process for preparing the same.
    The present invention further relates to a method for producing a poly (alkylene oxide) by polymerizing an alkylene oxide in the presence of phosphine sulfide.
    Poly (alkylene oxide) is an important polymer as a starting material for polyurethane foams or elastomers or by surfactants, for example by reacting with isocyanates.
    The present invention also relates to a method for producing 1,2-dioxyethane derivatives by reacting an epoxy compound with a carboxylate, carboxylic anhydride, carbonate or phenol compound in the presence of phosphine sulfide. These 1,2-dioxyethane derivatives are very important compounds as starting materials for polymer materials or intermediates for medicines or pesticides.
    The hydroxides or carbonates of alkali or alkaline earth metals have been used as catalysts or reactants for various reactions because of their basicity. However, since they are generally insoluble in organic solvents and soluble in water, they are hardly applicable to reactions in organic solvents. Thus, 1,8-diazabicyclo [5.4.0] -7-undecene, 1,5-diazabicyclo [4.3.0] -5-nonene and 1,4-diazabicyclo [2.2.2] octane Various highly basic organic compounds, such as these, are disclosed.
    However, their basicity or catalysis based on their basicity is limited. Recently, organic compounds called phosphazene base groups consisting of carbon, hydrogen, nitrogen and phosphorus, strong bases with strong hydrogen withdrawing ability, have been discovered (Nachr. Chem. Tech. Lab., 38, 1214-1226 (1990)). .
    It is also disclosed that phosphazene bases act as effective catalysts for anionic polymerization of ethylene oxide using alcohols as initiators (Martin Moller et al., Macromol. Rapid Commun., 17, 143-148 (1996)). .
    The preparation of the phosphazene base requires a complicated process, and in this process, it is necessary to use a strong base such as potassium amide in order to make the phosphazene base a strong basic (Nachr. Chem. Tech. Lab., 38, 1216 (1990). Therefore, manufacture of a phosphazene base is not industrially advantageous. In addition, the base is prone to deterioration by carbon dioxide in the air due to its strong basicity, which causes problems in handling.
    Tris [tris (dimethylamino) phosphoranylideneamino] phosphine oxide is also known as a useful base (G. N. Koidan et al., Journal of general chemistry of the USSR, 55, 1453 (1985)). However, phosphine oxides are very absorbent and, for example, may absorb 7 to 8% by weight of moisture after storage for 24 hours in normal atmosphere (temperature: 18-24 ° C .; humidity: 52-59%). Can be. Its solubility in water is at least 50% by weight. Due to its high hygroscopicity, phosphine oxide can be used for limited applications as a catalyst and requires special precautions in handling to ensure stable catalysis.
    In order to produce poly (alkylene oxide) by polymerization of alkylene oxide, an alkali metal salt of an active hydrogen compound is formed from a basic alkali metal compound such as potassium hydroxide and active hydrogen compound such as polyhydric alcohol by dehydration before the start of polymerization. This method is common, and this method is used industrially.
    Other combinations of initiator systems are also disclosed. For example, U.S. Patent No. 3,829,505 discloses a method for producing a polymer of propylene oxide using a compound represented by Zn 3 [Fe (CN) 6 ] H 2 O. dioxane as an active hydrogen compound. . Japanese Patent Laid-Open No. 2-276821 discloses a method for producing a polymer by reacting a polyol prepared using a zinc-hexacyanocobaltate complex with sodium methoxide and then ethylene oxide. In addition, Japanese Unexamined Patent Publication No. 62-232433 discloses ethylene using a product prepared by adding a diethyl zinc solution in hexane to a dispersant of 1,4-butanediol and a nonionic surfactant in the fumed silica slurry in hexane. A method of polymerizing oxides to produce polymers is disclosed. However, these methods all contain metal components. Therefore, if the metal component remains in the poly (alkylene oxide) product, it may adversely affect the reaction during the preparation of the polyurethane or the physical properties of the polyurethane, so that the metal component is appropriately removed during poly (alkylene oxide) production. This requires special procedures or complex processing.
    On the other hand, Japanese Patent Application Laid-Open No. 50-159595 discloses a method for producing a polymer from ethylene oxide using an initiator system which is a combination of an alkane polyol as an active hydrogen compound and boron trifluoride etherate. However, for these initiator systems, it is known that certain impurities in the polymer adversely affect the physical properties of the polyurethane and require complicated treatment to properly remove it. Japanese Laid-Open Patent Publication No. 57-12026 discloses a method for producing a polymer of alkylene oxide using an alcohol and an aminophenol. In addition, Japanese Patent Laid-Open No. 56-38323 discloses a method for producing propylene oxide using sorbitol and tetramethylammonium hydroxide. However, these systems all have problems such as insufficient polymerization activity and residual amine odor.
    It is known to prepare poly (alkylene oxide) by polymerizing alkylene oxide in the presence of phosphazene base and active hydrogen compound (European Patent Publication No. 0763555; Macromol. Rapid Commun., Vol. 17, pp. 143-148 (1996); Macromol. Symp., Vol. 107, pp. 331-340 (1996)). The phosphazene base in this method is an initiator with strong basicity. However, it is necessary to employ a complicated process for the production of the phosphazene base, and to make the phosphazene base infectious in this process, it is necessary to use a strong base such as potassium amide. Therefore, the preparation of phosphazene base is not industrially advantageous. In addition, the base is easily deteriorated by carbon dioxide in the air due to its strong basicity, which causes problems in handling.
    In addition, EP 0791600 discloses a method for producing poly (alkylene oxide) by polymerizing alkylene oxide in the presence of a phosphazenium salt of an active hydrogen compound. In this method, before the start of polymerization, for example, an alkali metal hydroxide and an active hydrogen compound are used as an initiation system, and dephosphorization of the active hydrogen compound is required by dehydration or additional dehydration requiring additional equipment as in the above method. It is necessary to prepare the nium salt. In addition, since inorganic salts formed during the process can interfere with the successful progress of the polymerization, the salts need to be removed, making the manufacturing process more complicated. Therefore, this method needs to be industrially improved.
    For example, tertiary amines, quaternary ammonium salts and quaternary phosphonium salts improve the reaction of epoxy compounds with carboxylates, carboxylic anhydrides or carbonates to produce 1,2-dioxyethane derivatives. Known (K. Funabashi, Bulletin Chemical Society of Japan, vol. 52, p. 1488 (1979); Tadaomi Nishikubo; Journal of Organic Synthesis, vol. 49 (3), p. 219 (1991)). However, catalysts such as tertiary amines, quaternary ammonium salts and quaternary phosphonium salts exhibit inadequate activity. The catalyst may be used in an increased amount or concentration, or may be reacted under strict conditions to allow the reaction to proceed appropriately. However, such an operation causes problems such as side reactions, decomposition of reactants or products, resulting in inadequate yield or selectivity.
    It is also known to produce 1,2-dioxyethane derivatives by accelerating the reaction between an epoxy compound and a phenol compound with an acid such as boron trifluoride or a tertiary amine or tertiary phosphine. However, these conventional acids and base catalysts have a problem of having inadequate catalytic activity.
    It is an object of the present invention to provide an organic compound which is basic and soluble in the organic solvent, that is, soluble in organic solvents, which does not have any problems in the manufacturing or handling as described above and exhibits catalytic activity as a basic compound.
    Another object of the present invention is to provide a method for producing the compound.
    Another object of the present invention is a method for efficiently producing a poly (alkylene oxide) by polymerizing an alkylene oxide in the presence of the compound, which does not require any treatment prior to polymerization and does not cause odor of residual amines. To provide.
    It is still another object of the present invention to find a catalyst that is highly active in the reaction of an epoxy compound with a carboxylate, carboxylic anhydride, carbonate or phenol compound, and uses this catalyst to obtain a high yield of 1,2-dioxyethane derivatives. It is to provide an efficient method for manufacturing.
    The present inventors made an intensive attempt to achieve these objects and finally produced a phosphine sulfide suitable for solving the above problem, which is composed of carbon, hydrogen, nitrogen, phosphorus and sulfur atoms represented by the general formula (1).
    The first aspect of the present invention is general formula (1):

    Is a phosphine sulfide represented by (wherein R may be the same or different and each represents a hydrocarbon group having 1 to 10 carbon atoms).
    According to a second aspect of the present invention, 1 mol of thiophosphoryl chloride and general formula (2):

    Wherein phosphine represented by the general formula (1) is provided with a step of reacting 3 moles of phospholane represented by (wherein R may be the same or different and each represents a hydrocarbon group having 1 to 10 carbon atoms). It is a manufacturing method of an oxide. "Reaction of 1 mol of thiophosphoryl chloride and 3 mol of phosphoranes represented by general formula (2)" represents a stoichiometry in which three chlorine atoms in thiophosphoryl chloride are replaced by phosphorane, and thus, the actual production reaction It does not represent the ratio of the quantity between these in.
    The third aspect of the present invention is alkylene in the presence of an active hydrogen compound selected from phosphine sulfide represented by the general formula (1) or an organic compound having a partial structure of water and -OH or -NH-. It is a manufacturing method of the poly (alkylene oxide) characterized by including the process of superposing | polymerizing an oxide.
    In a fourth aspect of the present invention, there is provided a step of reacting an epoxy compound with a carboxylate, carboxylic anhydride, carbonate or phenol compound in the presence of phosphine sulfide represented by the general formula (1). Formula (3), (4), (5) or (6):


    The carbon atom C- or -C attached to a carbonyl group or an oxygen atom belongs to an aliphatic, cycloaliphatic or aromatic hydrocarbon, and is a method for producing 1,2-dioxyethane derivatives having a partial structure.
    1 shows 31 P-NMR spectrum (solvent: DMSO-d 6 ) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide
    2 is a 1 H-NMR spectrum (solvent: DMSO-d 6 ) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide
    3 is an IR spectrum (solvent: DMSO-d 6 ) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide by KBr pellet method;
    Hereinafter, preferred embodiments of the present invention will be described in detail.
    Formula (1) is a limiting structure for phosphine sulfide in the present invention in which the phosphorus atom and the sulfur atom are bonded via a double bond, but alternatively, the compound has a cation form in which the phosphorus atom is a c + - It may have a restriction structure in which electrons concentrate on sulfur atoms and form anions while having S − . The positive charges on the personnel may be localized throughout the molecule through conjugated bonds. Therefore, it should be noted that the phosphine sulfide represented by the general formula (1) is a resonance hybrid including all of the above restriction structures.
    The first and second aspects will be described below. R in phosphine sulfide represented by General formula (1) may be same or different, and is methyl group, ethyl group, n-propyl group, isopropyl group, allyl group, n-butyl group, sec-butyl group, tert-, respectively. Butyl group, 2-butenyl group, 1-pentyl group, 2-pentyl group, 3-pentyl group, 2-methyl-1-butyl group, isopentyl group, tert-pentyl group, 3-methyl-2-butyl group, Neopentyl group, n-hexyl group, 4-methyl-2-pentyl group, cyclopentyl group, cyclohexyl group, 1-heptyl group, 3-heptyl group, 1-octyl group, 2-octyl group, 3-ethyl- 1-hexyl group, 1,1-dimethyl-3,3-dimethylbutyl group (common name; tert-octyl group), nonyl group, decyl group, phenyl group, 4-tolyl group, benzyl group, 1-phenylethyl group and 2- C1-C10 hydrocarbon group containing aliphatic, alicyclic, and aromatic hydrocarbon groups, such as a phenylethyl group, is shown. Alternatively, two R's attached to the same nitrogen atom may combine with each other to form a ring structure.
    R is preferably a methyl group, an ethyl group or an n-propyl group, and more preferably a methyl group.
    Phosphine sulfide represented by the general formula (1) is a novel unknown compound, and neither its preparation method nor its catalysis is presented or suggested in any known literature.
    The phosphine sulfide represented by the general formula (1) may be prepared by reacting 1 mol of thiophosphoryl chloride with 3 mol of the phosphorane represented by the general formula (2), and the reaction is represented by the following formula (7):
    Cl 3 P = S + 3 (R 2 N) 3 P = NH → [(R 2 N) 3 P = N] 3 P = S + 3HCl... (7)
    Can be displayed as
    In the process of the present invention, the actual amount of phosphorane represented by the general formula (2) to 1 mol of thiophosphoryl chloride is usually at least 3 mol, preferably 3 to 20 mol, more preferably 6 to 8 mol to be. Another basic compound may exist as a receptor for hydrogen chloride which is a by-product of the reaction. Alternatively, at least 6 moles of phosphorane is present so that an excess of phosphorane is used as a hydrochloride susceptor, so that the phosphorus after hydrogen chloride accepts a form of phosphonium chloride (R 2 N) 3 P + (NH 2 ) Cl − . You may get drunk.
    The reaction temperature is usually -30 to 250 ° C, preferably 0 to 200 ° C, more preferably 20 to 150 ° C. The reaction temperature may be raised stepwise, for example, from the low temperature of the initial stage to the elevated temperature of the late stage. The reaction may be carried out under reduced pressure, atmospheric pressure or increased pressure, usually under atmospheric pressure.
    The reaction period depends on various factors such as the reaction temperature, but is usually 0.1 to 100 hours, preferably 1 to 50 hours, more preferably 2 to 30 hours.
    In the reaction, a solvent is generally used. Examples of the solvent used include saturated aliphatic and saturated alicyclic hydrocarbons such as pentane, hexane, cyclohexane, heptane, octane, nonane and decane; Benzene, toluene, o-xylene, m-xylene, p-xylene, ethylbenzene, n-propylbenzene, cumene, 1,2,3-trimethylbenzene, 1,2,4-trimethylbenzene, mesitylene, tetralin, Butylbenzene, p-cymene, cyclohexylbenzene, 1,2-diethylbenzene, 1,3-diethylbenzene, 1,4-diethylbenzene, 1,2-diisopropylbenzene, 1,3-diiso Unsubstituted or alkyl-substituted aromatic hydrocarbons such as propylbenzene, 1,4-diisopropylbenzene, 1,2,4-triethylbenzene, 1,3,5-triethylbenzene and dodecylbenzene; Chlorobenzene, o-dichlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, bromobenzene, o-dibrobenzene, m-dibromobenzene, 1-bromo-2-chlorobenzene Halogenated aromatic hydrocarbons such as 1-bromo-3-chlorobenzene, 1-bromonaphthalene and 1-chloronaphthalene; And 2-chlorotoluene, 3-chlorotoluene, 4-chlorotoluene, 2-bromotoluene, 3-bromotoluene, 2,4-dichlorotoluene, 3,4-dichlorotoluene, 1-bromo-2-ethyl Benzene, 1-Bromo-4-ethylbenzene, 1-chloro-2-ethylbenzene, 1-chloro-4-ethylbenzene, 1-chloro-4-isopropylbenzene, 1-bromo-4-isopropylbenzene And halogenated alkyl substituted aromatic hydrocarbons such as mesityl chloride, 4-chloro-o-xylene and 2-chloro-o-xylene.
    Other solvents may be used as long as they do not adversely affect the process of the present invention. As a preferable solvent, C7-C9 alkyl substituted aromatic hydrocarbons, such as toluene, o-xylene, m-xylene, p-xylene, ethylbenzene, and mesitylene; Chlorinated benzenes having 1 to 3 carbon atoms such as chlorobenzene, o-dichlorobenzene and 1,2,4-trichlorobenzene; And chlorinated alkylsubstituted aromatic hydrocarbons having 7 to 9 carbon atoms and 1 to 2 chlorine atoms such as 2-chlorotoluene, 2,4-dichlorotoluene, 1-chloro-4-ethylbenzene and mesityl chloride. have.
    You may use these solvent individually or in combination of 2 or more types. The amount of the solvent is not limited, but is usually less than 500 parts by weight, preferably 1 to 100 parts by weight, more preferably 1.5 to 20 parts by weight, per 1 part by weight of thiophosphoryl chloride as a starting material. It is also acceptable that the liquid thiophosphoryl chloride be partially insoluble.
    After the reaction, the phosphine sulfide represented by the general formula (1) generated may be separated by a conventional method. For example, the phosphonium chloride as a by-product usually precipitates as a solid in the reaction solution, and after removal by filtration, the filtrate may be washed with water. After evaporation of the solvent, phosphine sulfide is separated as a solid. If necessary, purification methods such as recrystallization may be performed.
    Thus, the phosphine sulfide represented by General formula (1) can be manufactured by the convenient process of this invention. Phosphine sulfide is dissolved in nonpolar to polar organic solvents. Surprisingly, phosphine oxide was found to be not absorbent at all.
    Absorption test for 48 hours under normal atmospheric pressure (temperature: 18-24 ° C .; humidity: 52-59%) shows that Tris [tris (dimethylamino) phosphora, a compound represented by the general formula (1) wherein R is a methyl group Nilideneamino] phosphine sulfide did not increase the weight by water absorption. Phosphine sulfide is considerably advantageous in handling as compared to tris [tris (dimethylamino) phosphoranylideneamino] phosphine oxide which has absorbed 7 to 8% by weight of water for 24 hours under the above conditions. Phosphine sulfide is quite insoluble in water, but may provide 0.003 M aqueous solution. The pH of the low aqueous solution is pH 11.25 which indicates that the phosphine sulfide is basic.
    Phosphine sulfide represented by the general formula (1), for example, as described later, a method for producing a poly (alkylene oxide) by polymerizing alkylene oxide or an epoxy compound, carboxylate, carboxylic anhydride, carbonate Or it is very useful in the method of manufacturing a 1, 2- dioxyethane derivative by reacting a phenolic compound.
    Hereinafter, the third aspect of the present invention will be described.
    The third aspect of the present invention is alkylene in the presence of an active hydrogen compound selected from phosphine sulfide represented by the general formula (1) or an organic compound having a partial structure of water and -OH or -NH-. It is a manufacturing method of the poly (alkylene oxide) characterized by including the process of superposing | polymerizing an oxide.
    In the above method of the present invention, the phosphine sulfide represented by the general formula (1) can react with an alkylene oxide and / or an active hydrogen compound to form a derivative of phosphine sulfide to act as an initiator. In the polymerization of alkylene oxide, the use of such derivatives of phosphine sulfide prepared in advance or separately is, in the concept of the present invention, phosphine sulfide represented by the general formula (1) or the phosphine sulfide and water and- Polymerizing an alkylene oxide in the presence of an active hydrogen compound selected from organic compounds having a substructure of OH or -NH-.
    The alkylene oxide in the manufacturing method of a poly (alkylene oxide) is ethylene oxide, a propylene oxide, 1,2-butylene oxide, 2, 3- butylene oxide, styrene oxide, cyclohexene oxide, epichlorohydrin And a tertiary ethoxy group such as epibromohydrin, methylglycidyl ether, allyl glycidyl ether, and phenylglycidyl ether. Other alkylene oxides may be used as long as they do not adversely affect the method of the present invention. These may be used in combination of 2 or more type, 2 or more types of alkylene oxide may be used simultaneously or sequentially, or may repeat these use sequentially.
    The alkylene oxide is preferably ethylene oxide, propylene oxide, 1,2-butylene oxide or styrene oxide, more preferably ethylene oxide or propylene oxide, even more preferably propylene oxide.
    The active hydrogen compound in the method for producing poly (alkylene oxide) is a compound selected from water and organic compounds having a partial structure of -OH or -NH-.
    Moreover, water may be sufficient. Examples of the organic compound having a partial structure of —OH include formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, lauric acid, stearic acid, oleic acid, phenylacetic acid, dihydrocinnamic acid, cyclohexanecarboxylic acid, benzoic acid and p-methylbenzoic acid. And carboxylic acids having 1 to 20 carbon atoms such as 2-carboxynaphthalene; 2-20 carbon atoms, such as oxalic acid, malonic acid, succinic acid, maleic acid, fumaric acid, adipic acid, itaconic acid, butanetetracarboxylic acid, phthalic acid, isophthalic acid, terephthalic acid, trimellitic acid and pyromellitic acid, and 2-6 carboxyl groups Polycarboxylic acids having; Carbamic acids such as N, N-diethylcarbamic acid, N-carboxypyrrolidone, N-carboxaniline and N, N'-dicarboxy-2,4-toluenediamine; Methanol, ethanol, n-propanol, isopropanol, n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, isopentyl alcohol, tert-pentyl alcohol, n-octyl alcohol, lauryl alcohol, cetyl alcohol, cyclopentanol, Alcohols having 1 to 20 carbon atoms such as cyclohexanol, allyl alcohol, crotyl alcohol, methylvinylcarbinol, benzyl alcohol, 1-phenylethyl alcohol, triphenylcarbinol and cinnamil alcohol; Ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, 1,4-cyclohexanediol, trimethylol Polyhydric alcohols having 2 to 20 carbon atoms and 2 to 8 hydroxyl groups such as propane, glycerin, diglycerin, trimethylolmelamine, pentaerythritol, and dipentaerythritol; Sugars and derivatives thereof such as glucose, sorbitol, dextrose, fructose and sucrose; Aromatic compounds having 6 to 20 carbon atoms and 1 to 3 hydroxyl groups such as phenol, 2-naphthol, 2,6-dihydronaphthalene and bisphenol-A; And poly (alkylene oxides) having from 2 to 8 terminals and poly (ethylene oxide), poly (propylene oxide) and copolymers thereof, and having 1 to 8 hydroxyl groups at their terminals and having a number average molecular weight of 200 to 50,000. And the like.
    Organic compounds having a partial structure of -NH- as an active hydrogen compound include methylamine, ethylamine, n-propylamine, isopropylamine, n-butylamine, isobutylamine, sec-butylamine, tert-butylamine, Aliphatic and aromatic primary amines having 1 to 20 carbon atoms such as cyclohexylamine, benzylamine, β-phenylethylamine, aniline, o-toluidine, m-toluidine and p-toluidine; Dimethylamine, methylethylamine, diethylamine, di-n-propylamine, ethyl-n-butylamine, methyl-sec-butylamine, dipentylamine, dicyclohexylamine, N-methylaniline and diphenylamine, etc. Aliphatic and aromatic secondary amines having 2 to 20 carbon atoms; Ethylenediamine, di (2-aminoethyl) amine, hexamethylenediamine, 4,4'-diaminodiphenylmethane, melamine, tri (2-aminoethyl) amine, N, N'-dimethylethylenediamine and di (2 Polyamines having 2 to 20 carbon atoms and 2 to 3 primary or secondary amino groups, such as -methylaminoethyl) amine; Saturated ring secondary amines having 4 to 20 carbon atoms such as pyrrolidine, piperidine, morpholine, and 1,2,3,4-tetrahydroquinoline; Unsaturated cyclic secondary amines having 4 to 20 carbon atoms such as 3-pyrroline, pyrrole, indole, carbazole, imidazole, pyrazole and purine; Cyclic polyamines having 4 to 20 carbon atoms and 2 to 3 secondary amino groups such as piperazine, pyrazine and 1,4,7-triazacyclononane; Unsaturated or N-monosubstituted amides having 2 to 20 carbon atoms such as acetamide, propionamide, N-methylpropionamide, N-methylbenzamide and N-ethylstearylamide; 5- to 7-membered ring amides such as 2-pyrrolidone and ε-caprolactam; And dicarboxylic acid amides having 4 to 10 carbon atoms such as succinimide, maleimide, and phthalimide.
    As an active hydrogen compound, the compound which has some active hydrogen is mentioned. The polymerization is usually started from the anion moiety generated after removing all the active hydrogen compounds as protons.
    As an active hydrogen compound, an organic compound having a partial structure of —OH includes methanol, ethanol, n-propanol, isopropanol, n-butyl alcohol, sec-butyl alcohol, tert-butyl alcohol, iso-pentyl alcohol, tert-pentyl alcohol, n-octyl alcohol, lauryl alcohol, cetyl alcohol, cyclopentanol, cyclohexanol, allyl alcohol, crotyl alcohol, methylvinylcarbinol, benzyl alcohol, 1-phenylethyl alcohol, triphenylcarbinol and cinnamil alcohol, etc. Alcohols having 1 to 20 carbon atoms; Ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,6-hexanediol, 1,4-cyclohexanediol, trimethylol Polyhydric alcohols having 2 to 20 carbon atoms and 2 to 8 hydroxyl groups, such as propane, glycerin, diglycerin, pentaerythritol, and dipentaerythritol; Sugars and derivatives thereof such as glucose, sorbitol, dextrose, fructose and sucrose; And poly (alkylene oxides) having from 2 to 8 terminals and poly (ethylene oxide), poly (propylene oxide) and copolymers thereof, and having 1 to 8 hydroxyl groups at their terminals and having a number average molecular weight of 200 to 50,000. And the like.
    Preferred organic compounds having a partial structure of -NH- include ethylenediamine, di (2-aminoethyl) amine, hexamethylenediamine, 4,4'-diaminodiphenylmethane, tri (2-aminoethyl) amine, N Polyamines having 2 to 20 carbon atoms and 2 to 3 primary or secondary amino groups, such as, N'-dimethylethylenediamine, N, N'-diethylethylenediamine and di (2-methylaminoethyl) amine; Saturated ring secondary amines having 4 to 20 carbon atoms such as pyrrolidine, piperidine, morpholine, and 1,2,3,4-tetrahydroquinoline; And cyclic polyamines having 4 to 10 carbon atoms and 2 to 3 secondary amino groups such as piperazine, pyrazine and 1,4,7-triazacyclononane.
    As the organic compound having a partial structure of -OH, more preferably, as an active hydrogen compound, carbon number such as ethylene glycol, propylene glycol, 1,4-butanediol, trimethylolpropane, glycerin, pentaerythritol and dipentaerythritol Polyhydric alcohols having 2 to 20 and 2 to 8 hydroxyl groups; Sugars and derivatives thereof such as glucose, sorbitol, dextrose, fructose and sucrose; And poly (alkylene oxide) having 2 to 6 terminals and poly (ethylene oxide), poly (propylene oxide) and copolymers thereof, and 2 to 6 hydroxyl groups at their ends and their number average molecular weights of 200 to 10,000. And the like.
    The amount of the phosphine sulfide represented by the general formula (1) is not limited, but is usually 1 × 10 -15 to 5 × 10 -1 moles, preferably 1 × 10 -7 to 1, per mole of alkylene oxide. X10 -1 moles.
    The amount of the active hydrogen compound is not limited, but is usually 1 to 1 × 10 5 mol, preferably 5 to 1 × 10 4 mol, more preferably 10 to 1 × 10 3 mol with respect to 1 mol of phosphine sulfide. to be.
    Although the polymerization method is not limited, the reaction vessel filled with a phosphine sulfide or a phosphine sulfide and an active hydrogen compound represented by the general formula (1) together with a solvent when using a solvent partially contains alkylene oxide, What is necessary is just to implement according to the method which introduces intermittently or continuously.
    The polymerization temperature depends on various factors such as the type of alkylene oxide used, the amount of phosphine sulfide represented by the general formula (1), and the type and amount of the active hydrogen compound, but is usually 150 ° C. or less, preferably 10 To 130 ° C, more preferably 50 to 120 ° C. The reaction pressure depends on various factors such as the type of alkylene oxide used, the type and amount of active hydrogen compound and the polymerization temperature, but is usually 3.0 MPa (absolute pressure expressed in megapascals; the same definition is used below). , Preferably it is 0.01-1.5 MPa, More preferably, it is 0.1-1.0 MPa. The reaction period depends on the type and amount of the reactants, the polymerization temperature and the polymerization pressure, but is usually within 70 hours, preferably 0.1 to 30 hours, more preferably 0.5 to 24 hours.
    In the manufacturing method of the poly (alkylene oxide) of this invention, you may combine 2 or more types of alkylene oxides. Two or more kinds of alkylene oxides may be used simultaneously to polymerize to produce a relatively large number of random copolymers depending on the difference in reactivity between them. Moreover, you may polymerize using 2 or more types of alkylene oxides sequentially, and may produce the block copolymer which consists of blocks of 2 or more types of poly (alkylene oxides). For example, after completion of the polymerization of the first alkylene oxide, the second alkylene oxide may be polymerized as it is to produce a block copolymer composed of two different blocks. After completion of the polymerization of the second alkylene oxide, the first alkylene oxide may be polymerized again or the above procedure may be repeated to produce an alternating block copolymer. More complex block copolymers may be produced by combining three or more alkylene oxides as described above. Preferred copolymers are block copolymers composed of blocks of poly (propylene oxide) and poly (ethylene oxide) prepared by sequentially polymerizing propylene oxide and ethylene oxide as alkylene oxides.
    In the polymerization reaction, a solvent may be used if necessary. Examples of the solvent used include aliphatic hydrocarbons such as pentane, hexane, heptane and cyclohexane; Aromatic hydrocarbons such as benzene and toluene; Ethers such as diethyl ether, tetrahydrofuran, 1,3-dioxane and anisole; And aprotic polar solvents such as dimethyl sulfoxide, N, N-dimethylformamide, hexamethylphosphoramide and N, N'-dimethylimidazolidinone. Other solvents may be used as long as they do not adversely affect the polymerization reaction of the method of the present invention. You may perform superposition | polymerization in the manufacturing method of the poly (alkylene oxide) of this invention in atmosphere of inert gas, such as nitrogen and argon, as needed.
    The poly (alkylene oxide) produced by the method of the present invention may often be used directly as a starting material for polyurethane foams or elastomers or surfactants after removing the solvent when the solvent is used. However, inorganic acids such as hydrochloric acid, phosphoric acid and sulfuric acid are usually used; Organic carboxylic acids such as formic acid, acetic acid and propionic acid; carbon dioxide; Alternatively, it may be used after treatment with an acidic ion exchange resin.
    Usually, you may refine | purify by washing | cleaning with water, an organic solvent, or its mixture, for example.
    Hereinafter, the fourth aspect of the present invention will be described. In a fourth aspect of the present invention, there is provided a step of reacting an epoxy compound with a carboxylate, carboxylic anhydride, carbonate or phenol compound in the presence of phosphine sulfide represented by the general formula (1). It is a manufacturing method of the 1, 2- deoxyethane derivative | guide_body which has a partial structure represented by Formula (3), (4), (5) or (6).
    Epoxy compounds are organic compounds consisting of three-membered epoxy groups, and include, for example, aliphatic, cycloaliphatic and aromatic epoxy compounds composed of oxygen atoms of an epoxy group and carbon and hydrogen atoms; Aliphatic, alicyclic and aromatic epoxy compounds containing halogen atoms; Aliphatic, alicyclic and aromatic epoxy compounds having a keto group; Aliphatic, alicyclic and aromatic epoxy compounds having an ether bond; Aliphatic, alicyclic and aromatic epoxy compounds having an ester bond; Aliphatic, alicyclic and aromatic epoxy compounds having a tertiary amino group; And aliphatic, cycloaliphatic and aromatic epoxy compounds having a cyano group.
    Examples of specific epoxy compounds include ethylene oxide, propylene oxide, 1,2-epoxy butane, 2,3-epoxy butane, 1,2-epoxyhexane, 1,2-epoxy octane, 1,2-epoxydecane, 1,2 Epoxydodecane, 1,2-epoxytetedecane, 1,2-epoxyhexadecane, 1,2-epoxyoctadecane, 7,8-epoxy-2-methyloctadecane, 2-vinyloxirane, 2-methyl 2-vinyloxirane, 1,2-epoxy-5-hexene, 1,2-epoxy-7-octene, 1-phenyl-2,3-epoxypropane, 1- (1-naphthyl) -2,3 -Aliphatic epoxy compounds composed of oxygen and carbon and hydrogen atoms of epoxy groups such as epoxy propane, 1-cyclohexyl-3,4-epoxy butane, 1,3-butadiene dioxane and 1,2,7,8-diepoxyoctane logistics; Cyclopentene oxide, 3-methyl-1,2-cyclopentene oxide, cyclohexene oxide, cyclooctene oxide, α-pinene oxide, 2,3-epoxynorbornane, limonene oxide, cyclododecane epoxide and 2, Alicyclic epoxy compounds composed of oxygen, carbon and hydrogen atoms of an epoxy group such as 3,5,6, -diepoxynorbornane; Styrene oxide, 3-methylstyrene oxide, 1,2-epoxybutylbenzene, 1,2-epoxyoctylbenzene, stilbene oxide, 3-vinylstyrene oxide, 1- (1-methyl-1,2-epoxyethyl)- 3- (1-methylvinyl) benzene, 1,4-bis (1,2-epoxypropyl) benzene, 1,3-bis (1,2-epoxy-1-methylethyl) benzene and 1,4-bis ( Aromatic epoxy compounds composed of oxygen atoms of epoxy groups such as 1,2-epoxy-1-methylethyl) benzene and carbon and hydrogen atoms; Epifluorohydrin, epichlorohydrin, epibromohydrin, hexafluoropropylene oxide, 1,2-epoxy-4-fluorobutane, 1- (2,3-epoxypropyl) -4-fluorobenzene 1- (3,4-epoxybutyl) -2-fluorobenzene, 1- (2,3-epoxypropyl) -4-chlorobenzene and 1- (3,4-epoxybutyl) -3-chlorobenzene Halogenated aliphatic epoxy compounds; Halogenated alicyclic epoxy compounds such as 4-fluoro-1,2-cyclohexene oxide and 6-chloro-2,3-epoxybicyclo [2.2.1] heptane; Halogenated aromatic epoxy compounds such as 4-fluorostyrene oxide and 1- (1,2-epoxypropyl) -3-trifluorobenzene; 3-acetyl-1,2-epoxypropane, 4-benzoyl-1,2-epoxybutane, 4- (4-benzoyl) phenyl-1,2-epoxybutane and 4,4'-bis (3,4-epoxy Aliphatic epoxy compounds having a keto group such as butyl) benzophenone; Alicyclic epoxy compounds having a keto group such as 3,4-epoxy-1-cyclohexanone and 2,3-epoxy-5-oxobicyclo [2.2.1] heptane; Aromatic epoxy compounds having a keto group such as 3-acetylstyrene oxide and 4- (1,2-epoxypropyl) benzophenone; Glycidyl methyl ether, butyl glycidyl ether, 2-ethylhexyl glycidyl ether, allyl glycidyl ether, ethyl 3,4-epoxybutyl ether, glycidyl phenyl ether, glycidyl 4-tert-butyl Phenyl ether, glycidyl 4-chlorophenyl ether, glycidyl 4-methoxyphenyl ether, glycidyl 2-phenylphenyl ether, glycidyl 1-naphthyl ether, glycidyl 4-indolyl ether, glyc Cydyl N-methyl-α-quinolon-4-yl ether, ethylene glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, 1,2-diglycidyloxybenzene, 2,2-bis Aliphatic having ether bonds such as (4-glycidyloxyphenyl) propane, tris (4-glycidyloxyphenyl) methane, poly (oxypropylene) trioltriglycidyl ether and glycidyl ether of phenol novolac Epoxy compounds; Alicyclic epoxy compounds having ether bonds such as 1,2-epoxy-4-methoxycyclohexene and 2,3-epoxy-5,6-dimethoxybicyclo [2.2.1] heptane; Aromatic epoxy compounds having ether bonds such as 4-methoxy styrene oxide and 1- (1,2-epoxybutyl) -2-phenoxybenzene; Glycidylformate, glycidyl acetate, 2,3-epoxybutyl acetate, glycidyl butyrate, glycidyl benzoate, diglycidyl terephthalate, poly (glycidyl acrylate), poly (glycidyl) Aliphatic epoxy compounds having an ester bond such as dimethyl methacrylate), a copolymer of glycidyl acrylate with another monomer, and a copolymer of glycidyl methacrylate with another monomer; Alicyclic epoxy compounds having ester bonds such as 1,2-epoxy-4-methoxycarbonylcyclohexane and 2,3-epoxy-5-butoxycarbonylbicyclo [2.2.1] heptane; Ester bonds such as ethyl 4- (1,2-epoxyethyl) benzoate, methyl3- (1,2-epoxybutyl) benzoate and methyl3- (1,2-epoxybutyl) -5-phenylbenzoate Aromatic aromatic epoxy compounds; N, N-glycidylmethylacetamide, N, N-ethylglycidylpropionamide, N, N-glycidylmethylbenzamide, N- (4,5-epoxypentyl) -N-methylbenzamide, Aliphatic epoxy compounds having a tertiary amino group such as N, N-diglycidyl aniline, bis (4-diglycidylaminophenyl) methane and poly (N, N-glycidylmethylacrylamide); Alicyclic epoxy having a tertiary amino group such as 1,2-epoxy-3- (diphenylcarbamoyl) cyclohexane and 2,3-epoxy-6- (dimethylcarbamoyl) bicyclo [2.2.1] heptane Compounds; Aromatic epoxy compounds having a tertiary amino group such as 2- (dimethylcarbamoyl) styrene oxide and 4- (1,2-epoxybutyl) -4 '-(dimethylcarbamoyl) biphenyl; Aliphatic epoxy compounds having cyano groups such as 4-cyano-1,2-epoxybutane and 1- (3-cyanophenyl) -2,3-epoxybutane; And alicyclic epoxy compounds having a cyano group such as 2-cyanostyrene oxide and 6-cyano-1- (1,2-epoxy-2-phenylethyl) naphthalene.
    These compounds may have other bonds, substituents or heteroatoms as long as they do not adversely affect the method of the present invention.
    Preferred epoxy compounds include (a) aliphatic or aromatic epoxy compounds consisting of an oxygen atom of an epoxy group and carbon and hydrogen atoms; (b) aliphatic or aromatic epoxy compounds having ether bonds; Or (c) an aliphatic or aromatic epoxy compound having an ester bond.
    More preferable epoxy compounds include ethylene oxide, propylene oxide, 1,2-epoxy butane, 2,3-epoxy butane, 1,2-epoxy hexane, 1,2-epoxy octane, 1,2-epoxydecane, 1, 2-epoxydodecane, 1,2-epoxytetedecane, 1,2-epoxyhexadecane, 1,2-epoxyoctadecane, 7,8-epoxy-2-methyloctadecane, 2-vinyloxirane, 2- Methyl-2-vinyloxirane, 1,2-epoxy-5-hexene, 1,2-epoxy-7-octene, 1-phenyl-2,3-epoxypropane, 1- (1-naphthyl) -2, Aliphatic epoxy consisting of oxygen and carbon and hydrogen atoms of epoxy groups such as 3-epoxypropane, 1-cyclohexyl-3,4-epoxybutane, 1,3-butadienedioxane and 1,2,7,8-diepoxyoctane Compounds; Glycidyl methyl ether, butyl glycidyl ether, 2-ethylhexyl glycidyl ether, allyl glycidyl ether, ethyl 3,4-epoxybutyl ether, glycidyl phenyl ether, glycidyl 4-tert-butyl Phenyl ether, glycidyl 4-chlorophenyl ether, glycidyl 4-methoxyphenyl ether, glycidyl 2-phenylphenyl ether, glycidyl 1-naphthyl ether, glycidyl 4-indolyl ether, glyc Cydyl N-methyl-α-quinolon-4-yl ether, ethylene glycol diglycidyl ether, 1,4-butanediol diglycidyl ether, 1,2-diglycidyloxybenzene, 2,2-bis Aliphatic having ether bonds such as (4-glycidyloxyphenyl) propane, tris (3-glycidyloxyphenyl) methane, poly (oxypropylene) trioltriglycidyl ether and glycidyl ether of phenol novolac Epoxy compounds; Glycidylformate, glycidyl acetate, 2,3-epoxybutyl acetate, glycidyl butyrate, glycidyl benzoate, diglycidyl terephthalate, poly (glycidyl acrylate), poly (glycidyl) And aliphatic epoxy compounds having an ester bond such as dimethyl methacrylate), a copolymer of glycidyl acrylate with another monomer, and a copolymer of glycidyl methacrylate with another monomer.
    In the method of the present invention, 1,2-dioxyethane derivatives prepared by reacting an epoxy compound and a carboxylate in the presence of a phosphine sulfide represented by the general formula (1) are used for the ester bond in the carboxylate. Wherein the separated epoxy group in the epoxy compound is inserted between the acyl group and the alkoxy group or the aryloxy group, and the carbon atom C- or -C attached to the carbonyl group or the oxygen atom belongs to an aliphatic, alicyclic or aromatic hydrocarbon (3 It is a compound having a partial structure represented by).
    Examples of the carboxylates used include aliphatic, cycloaliphatic and aromatic carboxylates composed of ester-bonded oxygen atoms, carbohydrates and hydrogen atoms; Aliphatic, alicyclic and aromatic carboxylates; Aliphatic, alicyclic and aromatic carboxylates having an ether bond; Aliphatic, cycloaliphatic and aromatic carboxylates having a cyano group; And aliphatic, cycloaliphatic and aromatic carboxylates having a keto group.
    Examples of specific carboxylates include methyl formate, ethyl formate, methyl acetate, ethyl acetate, n-butyl acetate, isopropyl propionate, methyl butyrate, n-octyl butyrate, isobutyrate n-decyl, vinyl acetate, and methyl laurate Allyl stearate, cyclohexyl oleate, phenylacetic acid phenyl, 1,2-diacetoxyethane, triacetin, 1,2-diacetoxybenzene, 2,6-diacetoxynaphthalene, 4,4'-diacetox Cibiphenyl, 2,2-bis (4-acetoxyphenyl) propane, phenol novolac acetate, poly (butanediene) diol acetate, poly (isobutene) diol acetate, poly (vinyl acetate), poly (lactic acid), poly (Caprolactone), dimethyl oxalate, diethyl oxalate, dimethyl malonic acid, dimethyl succinate, diphenyl succinate, adipic acid dimethyl, adipic di-n-octyl, 1,10-decanedicarboxylic acid di (4-methylphenyl) , 1,2,3,4-butanetetracarboxylic acid tetra Phenyl, poly (butadiene) dicarboxylic acid dimethyl, poly (methylacrylate), poly (methylmethacrylate), copolymer of glycidyl acrylate with other monomers, air with glycidyl methacrylate with other monomers Aliphatic carboxylates comprising oxygen and carbon and hydrogen atoms of ester bonds such as coalescing, diethyl maleate, dimethyl fumarate, di-t-butyl fumarate and dimethyl itaconic acid; Cyclohexanecarboxylic acid 1-naphthyl, 2-norbornanecarboxylic acid ethyl, 2-norbornenecarboxylic acid phenyl, 1,2-cyclobutanedicarboxylic acid diethyl, 1,4-cyclohexanedicarboxylic acid diphenyl, 1,2, 4-cyclohexanetricarboxylic acid tri-n-octyl, 1,2,4,5-cyclohexanetetracarboxylic acid tetra-n-octyl, 2,5-norbornanedicarboxylic acid dimethyl, 5-norbornane-2,5, Alicyclic carboxylates comprising oxygen and carbon and hydrogen atoms of ester bonds such as 6-tricarboxylic acid trimethyl and 1,3-adamantane carboxylic acid ethyl; Methyl benzoate, octadecyl benzoate, 2-methylbutyl p-methylbenzoate, methyl 1-naphthalenecarboxylic acid, n-hexyl 2-naphthalenecarboxylic acid, 4,4'-dibenzoyloxybiphenyl, 2,2-bis (4-benzoyl Aromatic groups consisting of oxygen and carbon and hydrogen atoms of ester bonds such as oxyphenyl) propane, benzoic acid phenol novolak, dimethyl phthalate, dimethyl isophthalate, dimethyl diethyl terephthalate, tributyl tributyl, tetraoctyl pyromellitate and polyethylene terephthalate Carboxylates; 4-fluorophenyl acetate, 4-chlorobutyric acid methyl, 5-fluoro-2-hexanoic acid phenyl, pentafluorophenylacetic acid ethyl, 4-chlorophenylacetic acid 4-fluorophenyl, 1,2-diacetoxy- 3-chlorobenzene, 2,6-diacetoxy-3-bronaphthalene, 4,4'-diacetoxy-3,3 ', 5,5'-tetrabromobiphenyl, 2,2-bis (4 Halogenated aliphatic carboxyl such as acetoxy-3,5-dibromophenyl) propane and 2,2-bis (4-acetoxyphenyl) -1,1,1,3,3,3-hexafluoropropane Rates; 3-bromocyclohexanecarboxylic acid isopropyl, 3-fluorohexanecarboxylic acid pentafluorophenyl, 5-chloro-2-bicyclo [2.2.1] heptancarboxylic acid n-octyl, 1,4-cyclohexanedicarboxylic acid di ( Halogenated alicyclic carboxylates such as 4-iodophenyl) and 1,2,4-cyclohexanetricarboxylic acid tri (3-fluoro-n-octyl); Pentafluorophenyl acetate, 4-chlorophenyl 4-bromobenzoic acid, cyclohexyl 4-chlorobenzoic acid, methyl pentafluorobenzoic acid, 6-iodo-1-naphthalenecarboxylic acid t-butyl, 1,2-dibenzoyloxy- 3-chlorobenzene, 2,6-dibenzoyloxy-3-bromonaphthalene, 4,4'-dibenzoyloxy-3,3 ', 5,5'-tetrabromobiphenyl, 2,2-bis (4 Halogenated aromatic carboxyl such as -benzoyloxy-3,5-dibromophenyl) propane and 2,2-bis (4-benzoyloxyphenyl) -1,1,1,3,3,3-hexafluoropropane Rates; Methyl methoxyacetic acid, 4-methoxyphenyl acetate, 2-methoxypropionic acid n-octyl, 2-methoxypropionic acid 2-methoxyethyl, 4- (4-methylphenoxy) butyric acid ethyl, 3-phenoxyphenylacetic acid n-butyl, di (2-acetoxy) ethyl ether, dipropylene glycol acetate, pentaacetylglucose, poly (oxyethylene) diol acetate, poly (oxypropylene) triol acetate and 2,2'-ethylenedioxy-di Aliphatic carboxylates having ether bonds such as naphthyl acetate; Ether linkages such as 4-methoxycyclohexanecarboxylic acid 2-phenoxyethyl, 3-benzyloxycyclohexanecarboxylic acid n-octyl and 5,6-dimethoxy-2-bicyclo [2.2.1] heptancarboxylic acid t-butyl Alicyclic carboxylates having; 3-phenoxybenzoic acid cyclohexyl, benzoic acid 2-methoxyethyl, 4-phenoxybenzoic acid 3-butoxypropyl, di (2-benzoyloxy) ethyl ether, benzoic acid dipropylene glycol, 5-methoxyisophthalic acid n-hexa Aromatic carboxylates having ether bonds such as decyl and 4,4'-ethylenedioxybenzoic acid phenyl; Cyano groups such as methyl cyanoacetate, 2-cyanoethyl acetate, 4-cyanophenyl 2- (2- (3-cyanophenyl) propionic acid, 4-cyanophenyl acetate and 2-cyanocyclohexyl propionate Aliphatic carboxylates, cycloaliphatic carboxylate 4-cyanobutyl, 3-cyanocyclohexane carboxylic acid 2-cyanocyclohexyl and 5-cyano-2-norbornane carboxylic acid alicyclic having a cyano group Carboxylates: Aromatic carboxylates having cyano groups such as 3-cyanopropyl benzoate, 4-cyanophenyl 2-cyanobenzoate, phenyl 4-cyanobenzoate and ethyl 6-cyano-2-naphthalene carboxylic acid Aliphatic carboxylates having a keto group such as methyl glycolate, 3-oxobutyl acetate, acetoacetic acid 4-oxocyclohexyl, phenyl pyruvate and ethyl acetoacetate; methyl 3-oxo-1-cyclopentanecarboxylic acid, 4 Oxo Alicyclic carboxylates having a keto group such as 1-cyclohexanecarboxylic acid 3-oxobutyl, cyclohexanecarboxylic acid 4-oxocyclohexyl, and 3-acetyl-1-cyclohexanecarboxylic acid n-butyl; And aromatic carboxylates having keto groups such as naphthyl, 2-benzoylethyl benzoate, 2-oxobutyl 4-benzoylbenzoate, and 5-acetylnaphthalene-1-carboxylic acid naphthyl.
    These carboxylates are all compounds, and include aliphatic, alicyclic and aromatic carboxylates composed of oxygen bonds and carbon and hydrogen atoms of ester bonds; Aliphatic, alicyclic and aromatic carboxylates; Aliphatic, alicyclic and aromatic carboxylates having an ether bond; Aliphatic, cycloaliphatic and aromatic carboxylates having a cyano bond; And aliphatic, cycloaliphatic and aromatic carboxylates having a keto group. These substituents or functional groups may contain the carboxyl group part, a hydroxyl group part, or both these parts in an ester group. The hydroxyl group portion consisting of an ester group may be aliphatic, alicyclic or aromatic.
    The carboxylates for the process of the invention may have other substituents, functional groups or heteroatoms so long as they do not adversely affect the process of the invention.
    Preferred carboxylates are (a) the aliphatic and aromatic carboxylates consisting of oxygen atoms of ester bonds and carbon and hydrogen atoms; And (b) the aliphatic and aromatic carboxylates having an ether bond.
    More preferable carboxylates are methyl formate, ethyl formate, methyl acetate, ethyl acetate, n-butyl acetate, isopropyl propionate, methyl butyrate, n-octyl butyrate, n-decyl isobutyrate, vinyl acetate and methyl laurate Allyl stearate, cyclohexyl oleate, phenylacetic acid phenyl, 1,2-diacetoxyethane, triacetin, 1,2-diacetoxybenzene, 2,6-diacetoxynaphthalene, 4,4'-diacetox Cibiphenyl, 2,2-bis (4-acetoxyphenyl) propane, phenol novolac acetate, poly (butanediene) diol acetate, poly (isobutene) diol acetate, poly (vinyl acetate), poly (lactic acid), poly (Caprolactone), dimethyl oxalate, diethyl oxalate, dimethyl malonic acid, dimethyl succinate, diphenyl succinate, adipic acid dimethyl, adipic di-n-octyl, 1,10-decanedicarboxylic acid di (4-methylphenyl) , 1,2,3,4-butanetetracarboxylic acid tetraphenyl , Poly (butadiene) dicarboxylic acid dimethyl, poly (methylacrylate), poly (methylmethacrylate), copolymer of glycidyl acrylate with other monomers, copolymer of glycidyl methacrylate with other monomers Aliphatic carboxylates comprising oxygen and carbon and hydrogen atoms of ester bonds such as diethyl maleate, dimethyl fumarate, di-t-butyl fumarate and dimethyl itaconic acid; And methyl methoxyacetate, 4-methoxyphenyl acetate, 2-methoxypropionic acid n-octyl, 2-methoxypropionic acid 2-methoxyethyl, 4- (4-methylphenoxy) butyric acid ethyl, 3-phenoxyphenyl N-butyl acetate, di (2-acetoxy) ethyl ether, dipropylene glycol acetate, pentaacetylglucose, poly (oxyethylene) diol acetate, poly (oxypropylene) triol acetate and 2,2'-ethylenedioxy- And aliphatic carboxylates having ether bonds such as diphthacetic acid.
    In the method of the present invention, the 1,2-dioxyethane derivative prepared by reacting an epoxy compound with a carboxylic anhydride in the presence of a phosphine sulfide represented by the general formula (1) has an anhydrous epoxy group in the epoxy compound. A compound having a substructure represented by the general formula (4) which is inserted between an acyl group and an acyloxy group in the carboxylic acid anhydride group of a carboxylic acid and which is attached to a carbonyl group, belongs to an aliphatic, alicyclic or aromatic hydrocarbon. to be.
    Examples of the anhydrous carboxylic acid to be used include aliphatic, alicyclic and aromatic anhydrides consisting of oxygen atoms of anhydrous carboxylic acid groups and carbon and hydrogen atoms; Aliphatic, alicyclic and aromatic anhydrides having ether bonds; And aliphatic, cycloaliphatic and aromatic anhydrides having a keto group.
    Examples of specific carboxylic anhydrides include acetic anhydride, propionic anhydride, butyric anhydride, isobutyric anhydride, valeric anhydride, iso valeric anhydride, tetramethylacetic anhydride, hexanoic anhydride, heptanoic anhydride, decanoic anhydride, lauric anhydride, Palmitic anhydride, stearic anhydride, dococolic anhydride, oleic anhydride, linoleic anhydride, mixed acid from phenylacetic anhydride, subric acid and formic acid, mixed acid from subric acid and acetic acid, 1,6-di (formal Carboxylic anhydrides such as miloxycarbonyl) hexane, 1,6-di (acetoxycarbonyl) hexane, 1,8-di (acetoxycarbonyl) octane and poly (butadiene) dicarboxylic acid and anhydrous mixed acid from acetic acid Aliphatic anhydrous carboxylic acids consisting of oxygen atoms of groups and carbon and hydrogen atoms; Cyclobutanecarboxylic acid anhydride, cycloheptanocarboxylic acid anhydride, cyclohexanecarboxylic acid anhydride, cycloheptanocarboxylic acid anhydride, 1-adamantanecarboxylic acid anhydride, norbornane-2-carboxylic acid anhydride, norbornene-2-carboxylic acid anhydride, 1,4- Oxygen atoms of anhydrous carboxylic acid groups such as di (formyloxycarbonyl) cyclohexane, 1,3-di (acetoxycarbonyl) adamantane and 1,3,5-tri (acetoxycarbonyl) cyclohexane; Alicyclic anhydride carboxylic acids composed of carbon and hydrogen atoms; Benzoic anhydride, acetoxycarbonylbenzene, 4-butylbenzoic anhydride, 1-naphthalene carboxylic acid anhydride, 2-naphthalene carboxylic acid anhydride, 1-methylnaphthalene-2-carboxylic acid anhydride, anhydrous biphenylene carboxylic acid, 4-fluorocarboxylic acid, 9-anthracenecarboxylic acid anhydride, trimellitic anhydride, 1,3-di (formyloxycarbonyl) benzene, 1,4-di (acetoxycarbonyl) benzene, 1,3,4-tri (acetoxycarbonyl Carboxylic acid groups such as benzene, 1,3,5-tri (acetoxycarbonyl) benzene, 2,6-di (acetoxycarbonyl) naphthalene and 1,3,6-tri (acetoxycarbonyl) naphthalene Aromatic anhydrides consisting of oxygen atoms of carbon and carbon and hydrogen atoms; 2-methoxyacetic anhydride, 3-phenoxypropionic anhydride, glutaric anhydride, 8-butoxyoctanoic anhydride, di (2-acetoxycarbonyl) ethyl ether, di (2-acetoxycarbonylethoxy) Aliphatic anhydrides having ether bonds such as ethane and poly (oxypropylene) dicarboxylic acid and anhydrous mixed acid from acetic acid; 4-methoxycyclohexanecarboxylic acid anhydride, 3-phenoxycycloheptancarboxylic acid anhydride, 5,6-dimethoxynorbornane-2-carboxylic acid anhydride, 7-butoxynorbornene-2-carboxylic acid anhydride and 7-oxo anhydride Alicyclic anhydrides having an ether bond such as cyclo [2.2.1] hexane-2-carboxylic acid; 3-methoxybenzoic anhydride, 3,4-dimethoxybenzoic anhydride, 2-phenoxybenzoic anhydride, 3-phenoxybenzoic anhydride, 1,4-di (acetoxycarbonyl) -2-butoxybenzene, 1, 3,4-tri (acetoxycarbonyl) -5-phenoxybenzene, 1,3,5-tri (acetoxycarbonyl) -4-methoxybenzene and 2,6-di (acetoxycarbonyl)- Aromatic carboxylic anhydrides having ether bonds such as 1-isopropoxynaphthalene; Aliphatic anhydrides having a keto group such as pyruvic anhydride, 2-ketobutyric anhydride, 7-oxooctanoic anhydride, and 4-ketopimelic acid and mixed anhydride from acetic acid; And 4-acetylbenzoic anhydride, 4-benzoylbenzoic anhydride, 9-fluorenone-1-carboxylic acid, 9-fluorenone-2-carboxylic acid, 9-fluorenone-4-carboxylic acid and anthraquinone-2-carboxylic acid anhydride. And aromatic anhydride carboxylic acids having keto groups such as these. Carboxylic anhydrides for the process of the invention may have other substituents or heteroatoms so long as they do not adversely affect the process of the invention.
    Preferred carboxylic anhydrides are the aliphatic and aromatic carboxylic anhydrides composed of oxygen atoms of carbonic anhydride groups and carbon and hydrogen atoms.
    As more preferable carboxylic anhydrides, benzoic anhydride, acetoxycarbonylbenzene, 4-butylbenzoic anhydride, 1-naphthalene carboxylic acid anhydride, 2-naphthalene carboxylic acid anhydride, 1-methylnaphthalene-2-carboxylic acid anhydride, biphenylene carboxylic anhydride, 4-fluorocarboxylic acid anhydride, 9-anthracenecarboxylic acid anhydride, trimellitic anhydride, 1,3-di (formyloxycarbonyl) benzene, 1,4-di (acetoxycarbonyl) benzene, 1,3,4 -Tri (acetoxycarbonyl) benzene, 1,3,5-tri (acetoxycarbonyl) benzene, 2,6-di (acetoxycarbonyl) naphthalene and 1,3,6-tri (acetoxycarbonyl Aromatic anhydrous carboxylic acids which consist of an oxygen atom of carbonic anhydride groups, such as a) naphthalene, and carbon and a hydrogen atom are mentioned.
    In the method of the present invention, the 1,2-dioxyethane derivative prepared by reacting an epoxy compound and a carbonate in the presence of a phosphine sulfide represented by the general formula (1) has a separated epoxy group in the epoxy compound. It is inserted between the alkoxy- or aryloxycarbonyl group and the alkoxy or aryloxy group in the carbonate group, and the carbon atom C- or -C attached to the oxygen atom is represented by general formula (5) belonging to aliphatic, alicyclic or aromatic hydrocarbon. It is a compound having a partial structure.
    Examples of the carbonate used include aliphatic, cycloaliphatic and aromatic carbonates composed of oxygen atoms of carbonate groups and carbon and hydrogen atoms; Halogenated aliphatic, cycloaliphatic and aromatic carbonates; And aliphatic, cycloaliphatic and aromatic carbonates having ether bonds.
    Examples of specific carbonates include dimethyl carbonate, n-octylmethyl carbonate, di-n-butyl carbonate, 1,4-di (methoxycarbonyloxy) butane, 1,8-di (ethoxycarbonyloxy) octane, Aliphatic carbonates composed of oxygen atoms of carbonate groups such as poly (ethylene carbonate) and poly (propylene carbonate), and carbon and hydrogen atoms; Oxygen atoms of carbonate groups such as cyclohexyl isopropyl carbonate, dicyclohexyl carbonate, 1,4-di (methoxycarbonyloxy) cyclohexane, and 1,3,5-tri (methoxycarbonyloxy) cyclohexane; Alicyclic carbonates composed of carbon and hydrogen atoms; Methylphenylcarbonate, diphenylcarbonate, 1,4-di (methoxycarbonyloxy) benzene, 2,2-bis (4-methoxycarbonyloxyphenyl) propane, 2,2-bis (4-benzoyloxycarbonyl Aromatic carbonates composed of oxygen atoms of carbonate groups such as oxyphenyl) propane and phenol novolakmethyl carbonate and carbon and hydrogen atoms; 8-Fluorooctylmethylcarbonate, di (3-bromobutyl) carbonate, 1,4-di (methoxycarbonyloxy) -2-chlorobutane and 1,8-di (ethoxycarbonyloxy)- Halogenated aliphatic carbonates such as 4,5,6-trifluorooctane; Methyl4-iodophenylcarbonate, di (2-chlorophenyl) carbonate, 1,4-di (methoxycarbonyloxy-2,3,5,6-tetrabromobenzene, 2,2-bis (4- Halogenated aromatic carbonates such as methoxycarbonyloxy-3,5-dibromophenyl) propane and 2,2-bis (4-benzoyloxycarbonyloxy-3,5-dichlorophenyl) propane; Aliphatic carbonates having ether bonds such as (methoxycarbonyloxy) ethyl ether, poly (oxyethylene) diolmethylcarbonate, and poly (oxypropylene) triolmethylcarbonate; and di-4- (methoxycarbonyloxy) Aromatic carbonates having ether bonds such as phenyl ether and di-2- (methoxycarbonyloxy) -1-naphthyl ether, etc. The carbonates for the method of the present invention adversely affect the method of the present invention. It may have other substituents or heteroatoms as long as it does not.
    Preferred carbonates include (a) the aliphatic and aromatic carbonates consisting of oxygen atoms of carbonate groups and carbon and hydrogen atoms; And (b) the aliphatic and aromatic carbonates having an ether bond.
    More preferable carbonates include dimethyl carbonate, n-octylmethyl carbonate, di-n-butyl carbonate, 1,4-di (methoxycarbonyloxy) butane, 1,8-di (ethoxycarbonyloxy) octane, poly Aliphatic carbonates composed of oxygen atoms of carbonate groups such as (ethylene carbonate) and poly (propylene carbonate), and carbon and hydrogen atoms; Methylphenylcarbonate, diphenylcarbonate, 1,4-di (methoxycarbonyloxy) benzene, 2,2-bis (4-methoxycarbonyloxyphenyl) propane, 2,2-bis (4-benzoyloxycarbonyl Aromatic carbonates composed of oxygen atoms of carbonate groups such as oxyphenyl) propane and phenol novolakmethyl carbonate and carbon and hydrogen atoms; And aliphatic carbonates having ether bonds such as di-2- (methoxycarbonyloxy) ethyl ether, poly (oxyethylene) diolmethylcarbonate, and poly (oxypropylene) triolmethylcarbonate.
    In the method of the present invention, 1,2-dioxyethane derivatives prepared by reacting an epoxy compound and a phenol compound in the presence of a phosphine sulfide represented by the general formula (1) have a separated epoxy group in the epoxy compound. It is a compound having a partial structure represented by the general formula (6), which is inserted between the phenoxy group and the hydrogen atom of the compound and attached to the oxygen atom, wherein the carbon atom -C belongs to an aromatic hydrocarbon.
    Examples of the phenol compound used include phenol, cresol, 3-isopropylphenol, 4-butylphenol, 2-cyclopentylphenol, 2,3-dimethylphenol, 2,3,6-trimethylphenol, and 2,6-diisopropyl. Phenol, 3,5-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, 5-indanol, 5,6,7,8-tetrahydro-1-naphthol, naphthol, Nonylphenol, 4-hydroxystyrene, 4-hydroxy-α-methylstyrene, 1,1'-bi-2-naphthol, catechol, resorcinol, hydroquinone, 2-methylresorcinol, 4-hexyl Resorcinol, 2,6-dihydroxynaphthalene, bis (4-hydroxyphenyl) methane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy-3- Methylphenyl) propane, 2,2'-biphenol, 4,4'-biphenol, phenylhydroquinone, 1,3,5-trihydroxybenzene, 2,4-bis (4-hydroxyphenyl) -4- Methyl-1-pentene, 2,4,6-tris (4-hydroxyphenyl) -2,6-dimethyl-3-hexene, 5-hydroxy-3- (4-hydroxyphenyl) -1,1, 3-trimethyl-2,3-dihi Loindene, 5-hydroxy-3- (4-hydroxyphenyl) -2,6-dimethyl-3-hexene, tri (4-hydroxyphenyl) methane, phenol novolac, poly (4-hydroxystyrene) And phenolic compounds comprising oxygen and carbon and hydrogen atoms of phenolic hydroxyl groups such as poly (4-hydroxy-α-methylstyrene); 3-fluorophenol, 2-trifluoromethylphenol, 4-chlorophenol, 2-bromophenol, 2,6-difluorophenol, 4-fluol-2-methylphenol, 2,3,4- Trichlorophenol, 2,2-bis (4-hydroxy-3,5-dichlorophenyl) propane, 2,2-bis (4-hydroxyphenyl) -1,1,1,2,2,2-hexa Halogenated phenol compounds such as fluoropropane, octafluoro-4,4'-biphenol and 6,6'-dibromo-1,1'-bi-2-naphthol; 2-ethoxyphenol, 4- (phenoxymethyl) phenol, 3,4,5-trimethoxyphenol, 7-methoxy-2-naphthol, 4-benzyloxy-3-methoxyphenol and 3,3 ' Phenolic compounds having ether bonds such as-(ethylenedioxy) diphenol; 3-hydroxyacetophenol, 2- (2-oxopropyl) phenol, 4-hydroxybenzophenone, 1-hydroxy-2-acetonaphtone, 4,4'-dihydroxybenzophenone, 2,6- Phenolic compounds having keto groups, such as dihydroxyacetophenone and proletin; 4-acetoxymethylphenol, methylsalicylate, 4-hydroxybenzylacrylate, ethyl4-hydroxy-3-methoxycinnamate, 2-methoxycarbonyl-6-methyl-3-naphthol, 1, Phenol compounds having ester bonds such as 2-bis (4-hydroxybenzoyloxy) ethane and ethyl 3,4,5-trihydroxybenzoate; And 4-acetaminophenol, 3- (N, N-dimethylcarbamoyl) phenol, 4- (N, N-dimethylcarbamoyl) -3-methylphenol, N- (3-hydroxy-5-methyl ) Phenylacrylamide, N- (5-hydroxy-8-methyl-2-naphthyl) methacrylamide, N- (4-hydroxybenzyl) benzamide and N, N'-bis (4-hydroxyphenyl And phenol compounds having an amide bond such as) -5-methyl-1,3-benzenedicarboxamide. These compounds may have other substituents or heteroatoms as long as they do not adversely affect the process of the present invention.
    Preferred phenolic compounds include (a) phenol, cresol, 3-isopropylphenol, 4-butylphenol, 2-cyclopentylphenol, 2,3-dimethylphenol, 2,3,6-trimethylphenol, 2,6-di Isopropylphenol, 3,5-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, 5-indanol, 5,6,7,8-tetrahydro-1-naphthol, Naphthol, nonylphenol, 4-hydroxystyrene, 4-hydroxy-α-methylstyrene, 1,1'-bi-2-naphthol, catechol, resorcinol, hydroquinone, 2-methylresorcinol, 4 -Hexyl resorcinol, 2,6-dihydroxynaphthalene, bis (4-hydroxyphenyl) methane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy- 3-methylphenyl) propane, 2,2'-biphenol, 4,4'-biphenol, phenylhydroquinone, 1,3,5-trihydroxybenzene, 2,4-bis (4-hydroxyphenyl)- 4-methyl-1-pentene, 2,4,6-tris (4-hydroxyphenyl) -2,6-dimethyl-3-hexene, 5-hydroxy-3- (4-hydroxyphenyl) -1, 1,3-trimethyl-2,3-diha Droindene, 5-hydroxy-3- (4-hydroxyphenyl) -2,6-dimethyl-3-hexene, tri (4-hydroxyphenyl) methane, phenol novolac, poly (4-hydroxystyrene Phenol compounds composed of oxygen atoms of phenolic hydroxyl groups such as poly (4-hydroxy-α-methylstyrene), and carbon and hydrogen atoms; (b) 3-fluorophenol, 2-trifluoromethylphenol, 4-chlorophenol, 2-bromophenol, 2,6-difluorophenol, 4-fluoro-2-methylphenol, 2,3 , 4-trichlorophenol, 2,2-bis (4-hydroxy-3,5-dichlorophenyl) propane, 2,2-bis (4-hydroxyphenyl) -1,1,1,2,2, Halogenated phenolic compounds such as 2-hexafluoropropane, octafluoro-4,4'-biphenol and 6,6'-dibromo-1,1'-bi-2-naphthol; And (c) 2-ethoxyphenol, 4- (phenoxymethyl) phenol, 3,4,5-trimethoxyphenol, 7-methoxy-2-naphthol, 4-benzyloxy-3-methoxyphenol and And phenol compounds having ether bonds such as 3,3 '-(ethylenedioxy) diphenol.
    More preferable phenolic compounds include phenol, cresol, 3-isopropylphenol, 4-butylphenol, 2-cyclopentylphenol, 2,3-dimethylphenol, 2,3,6-trimethylphenol, 2,6-diisopropyl Phenol, 3,5-di-tert-butylphenol, 2,6-di-tert-butyl-4-methylphenol, 5-indanol, 5,6,7,8-tetrahydro-1-naphthol, naphthol, Nonylphenol, 4-hydroxystyrene, 4-hydroxy-α-methylstyrene, 1,1'-bi-2-naphthol, catechol, resorcinol, hydroquinone, 2-methylresorcinol, 4-hexyl Resorcinol, 2,6-dihydroxynaphthalene, bis (4-hydroxyphenyl) methane, 2,2-bis (4-hydroxyphenyl) propane, 2,2-bis (4-hydroxy-3- Methylphenyl) propane, 2,2'-biphenol, 4,4'-biphenol, phenylhydroquinone, 1,3,5-trihydroxybenzene, 2,4-di (4-hydroxyphenyl) -4- Methyl-1-pentene, 2,4,6-tri (4-hydroxyphenyl) -2,6-dimethyl-3-hexene, 5-hydroxy-3- (4-hydroxyphenyl) -1,1, 3-trimethyl-2,3-dihi Oxygen, carbon and hydrogen atoms of phenolic hydroxyl groups such as loindene, 5-hydroxy-3- (4-hydroxyphenyl) -2,6-dimethyl-3-hexene and tri (4-hydroxyphenyl) methane Phenolic compounds having 6 to 27 carbon atoms; And 3-fluorophenol, 2-trifluoromethylphenol, 4-chlorophenol, 2-bromophenol, 2,6-difluorophenol, 4-fluoro-2-methylphenol, 2,3,4 -Trichlorophenol, 2,2-bis (4-hydroxy-3,5-dichlorophenyl) propane, 2,2-bis (4-hydroxyphenyl) -1,1,1,2,2,2- And halogenated phenol compounds having 6 to 15 carbon atoms, such as hexafluoropropane and octafluoro-4,4'-biphenol.
    In the method of the present invention, the epoxy compound is reacted with a carboxylate, carboxylic anhydride, carbonate or phenol compound in the presence of phosphine sulfide represented by the general formula (1). A carboxylate, carboxylic anhydride, a carbonate, or a phenol compound can be used individually or in combination of 2 or more types. In the latter case, the compound which preferentially reacts with the epoxy compound may depend on the reactivity of the compound used.
    In the method of the present invention, the epoxy compound may have both an epoxy group and a carboxylate, carboxylic anhydride, carbonate or phenolic hydroxyl group in one molecule. For such compounds, the reaction of the present invention takes place within the molecule. When such epoxy compounds react with separate carboxylates, carboxylic anhydrides, carbonates or phenolic compounds, whether the epoxy groups react intramolecularly or intermolecularly with the carboxylates, carboxylic anhydrides, carbonates or phenolic compounds depends on the reactivity of the compounds used. It depends on, so you can't usually decide.
    The reaction may be performed as long as the procedure ensures effective contact between the phosphine sulfide represented by the general formula (1), the epoxy compound, and the carboxylate, carboxylic anhydride, carbonate or phenol compound. In addition, the reaction may be carried out continuously in a batchwise or semi-batch manner. The reaction is usually carried out by contacting a phosphine sulfide, an epoxy compound, and a carboxylate, carboxylic anhydride, carbonate or phenol compound together; By adding an epoxy compound to a mixture of phosphine sulfide and carboxylate, carboxylic anhydride, carbonate or phenol compound; By adding phosphine sulfide to a mixture consisting of an epoxy compound and a carboxylate, carboxylic anhydride, carbonate or phenol compound; Or you may carry out by adding a carboxylate, carboxylic anhydride, a carbonate, or a phenol compound to the mixture which consists of a phosphine sulfide and an epoxy compound. The reactants may be added in part, intermittently or continuously.
    The ratio of carboxylate, carboxylic anhydride, carbonate or phenol compound to epoxy compound is usually 0.5 to 1.5 moles of carboxylate, carboxylic anhydride, carbonate or phenolic hydroxyl group in the compound per mole of epoxy group in the epoxy compound. May be 0.7-1.3 mol.
    The amount of the phosphine sulfide represented by the general formula (1) is not limited, but is usually 0.5 mole or less per mole of epoxy group in the epoxy compound, preferably 1 × 10 -5 to 0.1 mole, more preferably in any reaction type. Preferably 1 × 10 −4 to 5 × 10 −2 moles.
    The reaction temperature varies depending on various factors such as the kind of reactant and the amount of phosphine sulfide represented by the general formula (1) in any kind of reaction, but is usually 250 ° C or lower, preferably 30 to 200 ° C. The reaction pressure varies depending on the kind of reactant in any kind of reaction, but is usually 3.0 MPa (absolute pressure; the same definition is used below), preferably 0.01 to 1.5 MPa, more preferably 0.1 to 1.0 MPa. The reaction period is usually 48 hours or less, preferably 0.1 minutes to 24 hours, more preferably 0.6 minutes to 10 hours. Reaction may be performed in atmosphere of inert gas, such as nitrogen and argon, as needed.
    In the method of this invention, when reaction is necessary, you may perform in a solvent. As a solvent used, Aliphatic and alicyclic hydrocarbons, such as n-pentane, n-hexane, and a cyclohexane; Dimethyl ether, diethyl ether, diisopropyl ether, dibutyl ether, tetrahydrofuran, 1,4-dioxane, ethylene glycol dimethyl ether, diethylene glycol dimethyl ether, anisole, o-dimethoxybenzene, ethylphenyl ether Ethers such as butylphenyl ether and o-diethoxybenzene; Benzene, toluene, xylene, ethylbenzene, cumene, mesitylene, tetralin, butylbenzene, p-cymene, diethylbenzene, diisopropylbenzene, triethylbenzene, cyclohexylbenzene, dipentylbenzene and dodecylbenzene Aromatic hydrocarbons; Chlorobenzene, o-dichlorobenzene, m-dichlorobenzene, 1,2,4-trichlorobenzene, bromobenzene, o-dibromobenzene, bromochlorobenzene, o-chlorotoluene, p-chlorotoluene, p Aromatic hydrocarbons such as -chloroethylbenzene and 1-chloronaphthalene; And aprotic polar solvents such as dimethyl sulfoxide, N, N-dimethylformamide, hexamethylphosphoramide and N, N'-dimethylimidazolidinone. Other solvents may be used as long as they do not adversely affect the method of the present invention. You may use these solvent individually or in combination of 2 or more types.
    The method of separating the target 1,2-dioxyethane derivative from the reaction solution depends on the type of the reactant used, the type of the target 1,2-deoxyethane derivative, and the type and amount of the solvent used. In the case where a reaction liquid or a solvent is usually used, the desired 1,2-dioxyethane derivative may be separated from the residual liquid after evaporation of the solvent by a suitable separation method such as distillation, recrystallization, column chromatography, and the like.
    As described above, in the presence of phosphine sulfide represented by the general formula (1), the epoxy compound is reacted with a carboxylate, carboxylic anhydride, carbonate or phenol compound to produce the desired 1,2-dioxyethane derivative. It can be produced conveniently and efficiently.
    Hereinafter, although the first to fourth aspects of the present invention will be described in more detail by various examples, it should be noted that these various examples are merely illustrative and are not restrictive.
    First, the first and second aspects of the present invention will be described.
    Example 1
    Into a 100 cc flask in a nitrogen atmosphere, 4.474 g (26.41 mmol) of thiophosphoryl chloride (Aldrich) and 45.24 g (0.3078 mol) of o-dichlorobenzene dried up to 10 ppm of water on molecular sieves 3A were added. After adding 29.36 g (164.7 mmol) of iminotris (dimethylamino) phosphorane (Fluka) to the stirred mixture while controlling the internal temperature to 40 ° C. over 20 minutes, the mixture was held at 40 ° C. for 40 minutes. It was. Next, the mixture was heated to 70 ° C. and reacted at that temperature for 20 hours to obtain a white suspension. After cooling this suspension to ambient temperature, it filtered and obtained the white solid.
    The cationic portion of the - Dry the filtered white solid was analyzed by mass spectrometry, amino-tris (dimethylamino) phosphonium chloride {[(CH 3) 2 N ] 3 P + (NH 2) Cl} Molecular ion peaks were observed at 179, corresponding to molecular weight.
    The filtrate was washed three times with about 14 g of water. The o-dichlorobenzene phase was concentrated by vacuum drying to give a dark blue solid (11.50 g; crude yield: 73%). Next, 9.64 g of this solid was added to 15.24 g of n-hexane, and the mixture was heated to 50 ° C. to completely dissolve the solid. The obtained solution was cooled to 18 ° C. to precipitate crystals, filtered, dried at 50 ° C./1 mmHg, and tris [tris (dimethylamino) phosphoranilidene, which is a compound represented by the general formula (1) wherein R is a methyl group. 4.15g (melting point: 90.0-92.5 degreeC) was obtained as an amino] phosphine sulfide as white solid. Elemental analysis data of this white solid were as follows;
    Observations: C: 36.77, H: 9.47, N: 28.28, P: 21.01
    Calculated: C: 36.38, H: 9.18, N: 28.29, P: 20.85.
    A part of the white crystals was dissolved in DMSO-d 6 and 31 P-NMR spectroscopic measurement was performed. The results are shown in FIG. 1, where the chemical shift for personnel in the tri-n-butylphosphate used for quantitative analysis was set to 0.312 ppm. Under these conditions, the chemical shift for the occupants in orthophosphoric acid commonly used as a standard was found at 0.00 ppm.
    As can be seen in FIG. 1, the quartet and the doublet are at 17.1 ppm and 12.2 ppm, respectively, which are derived from two different persons in tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide Integral strength ratio is 1: 3. The quartet at 17.1 ppm corresponds to a single atom bound to the central sulfur atom of the molecule, while the double line at 12.2 ppm corresponds to three surrounding personnel. The quartet at 17.1ppm is observed because the central personnel combine with the surrounding three personnel, while the double line at 12.2ppm is observed because the surrounding personnel combine with the central personnel.
    2 and 3 show the 1 H-MNR spectrum and the IR spectrum by KBr pellet method in a DMSO-d 6 solution of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide, respectively. .
    Hereinafter, the manufacturing method of the poly (alkylene oxide) as a 3rd aspect of this invention is demonstrated.
    Example 2
    In a 400 ml autoclave equipped with a temperature probe, pressure gauge and stirrer, 1.03 g (1.73 mmol) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide, 13.1 g (142 mmol) of glycerine and 129 g (2.22) of propylene oxide mmol) was added and the atmosphere of this system was replaced with nitrogen. The mixture was heated to 80 ° C. and held at this temperature for 17 hours with a maximum pressure of 0.3 MPa (absolute pressure expressed in megapascals; hereafter using the same definition). At the end of the reaction, the pressure was 0.01 MPa. After purging the residual pressure while introducing nitrogen gas into the gas, the mixture was transferred to another vessel. The mixture was kept at 80 ° C. for 30 minutes under reduced pressure of 10 mmHg to remove volatiles. Next, nitrogen was introduced to the system to atmospheric pressure, the mixture was cooled to ambient temperature, and polyoxypropylene containing tris [tris (dimethylamino) phosphoranilideneamino] phosphine sulfide as a transparent and odorless liquid. 125 g of triol were obtained.
    Next, 33.2 g of the liquid was put into a 400 ml autoclave equipped with a temperature probe, a pressure gauge, a stirrer, and an inlet for alkylene oxide, the atmosphere of this system was replaced with nitrogen, and the mixture was heated to 80 deg. 197 g (3.39 mol) of propylene oxide were continuously introduced over 9 hours while controlling the reaction pressure to 0.4 MPa or less. After the completion of the feed, the mixture was further reacted at 80 ° C for 16 hours. At the end of the reaction, the pressure was reduced to 0.05 MPa. After purging the residual pressure while introducing nitrogen gas into the gas, the mixture was transferred to another vessel. The mixture was kept at 80 ° C. for 30 minutes under reduced pressure of 10 mmHg to remove volatiles.
    Next, nitrogen was introduced into the system to atmospheric pressure, and the mixture was cooled to ambient temperature to obtain 220 g of polypropylene triol as a transparent and odorless liquid. The hydroxyl value of this polymer (the amount of terminal hydroxyl groups expressed in mg of equimolar amount of KOH having hydroxyl groups per gram of polymer) was 28.5, and the estimated number average molecular weight was 5900. The molecular weight distribution (Mw / Mn) was 1.05 according to gel permeation chromatography using poly (ethylene oxide) as a standard.
    Example 3
    Into a 400 ml polymerization reactor as described in Example 2, 1.68 g (2.82 mmol) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide and 29.1 g (217 mmol) of dipropylene glycol were added. After replacing the atmosphere with nitrogen, the mixture was heated to 90 ° C., and 197 g (3.39 mol) of propylene oxide was continuously introduced over 7 hours while controlling the reaction pressure to 0.45 MPa or less. The mixture was further reacted at 90 ° C for 12 hours. The pressure was reduced to 0.11 MPa. After purging the residual pressure while introducing nitrogen gas into the gas, the mixture was transferred to another vessel. The mixture was kept at 80 ° C. for 30 minutes under reduced pressure of 10 mmHg to remove volatiles. Next, nitrogen was introduced into the system to atmospheric pressure, and the mixture was cooled to ambient temperature to obtain 222 g of polyoxypropylene diol as a transparent, odorless liquid. Its hydroxyl value was 111 and the estimated number average molecular weight was 1010.
    Comparative Example 1
    The procedure of Example 3 was repeated except that tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide was omitted. No consumption of propylene oxide was observed. The weight of the contents of the reaction vessel was 29.7 g, which was actually the same as the weight of the injected dipropylene glycol, so that no polyoxypropylene diol was formed.
    Example 4
    88.2 g of polyoxypropylenetriol obtained in Example 2 having a hydroxyl value of 28.5 and containing a catalyst component instead of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide and dipropylene glycol was used. The procedure of Example 3 was repeated except that 140 g (2.41 mol) of oxide was introduced to obtain 221 g of a transparent, odorless polyoxypropylene triol having a hydroxyl value of 11.9 and a number average molecular weight of 14200.
    Example 5
    Instead of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide and dipropylene glycol, propylene was obtained by using 121 g of polyoxypropylene triol obtained in Example 2 having a hydroxyl value of 28.5 and containing a catalyst component. Instead of oxide, 25.1 g (0.570 mol) of ethylene oxide was introduced over 1 hour, and the procedure of Example 3 was repeated except that the reaction period was 8 hours. The transparent and odor having a hydroxyl value of 23.7 and a number average molecular weight of 7100 was obtained. 146 g of block copolymer of polyoxypropylene-polyoxyethylenetriol free was obtained.
    Example 6
    The amount of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide was 0.2777 g (0.466 mmol), and instead of dipropylene glycol, the hydroxyl value was 168 (number average molecular weight: 1002) and potassium hydroxide catalyst. The procedure of Example 3 was repeated except that 31.1 g of polyoxypropylene triol (MN-1000; manufactured by Mitsui Chemical Co., Ltd.) manufactured industrially was used and the reaction period was changed to 20 hours. 24.4 and 216 g of transparent and odorless polyoxypropylene triol having a number average molecular weight of 6900 were obtained.
    Example 7
    6.95 g (217 mmol) of methyl alcohol was used instead of dipropylene glycol, and the procedure of Example 3 was repeated except that the reaction period was 19 hours. Transparent and odorless polyoxy with a hydroxyl value of 63.0 and a number average molecular weight of 890 was repeated. 197 g of propylene monool was obtained.
    Example 8
    Except for using 39.1 g (217 mmol) of glucose instead of dipropylene glycol, the procedure of Example 3 was repeated to obtain 227 g of a transparent, odorless polyoxypropylene pentaol having a hydroxyl value of 270 and a number average molecular weight of 1040.
    Example 9
    Instead of dipropylene glycol, 19.6 g (217 mmol) of 1,4-butanediol was used, and 244 g (3.39 mol) of 1,2-butylene oxide was used instead of propylene oxide while maintaining the pressure below 0.25 MPa. Except for 20 hours, the procedure of Example 3 was repeated to obtain 251 g of a transparent and odorless polyoxybutylenediol having a hydroxyl value of 98.4 and a number average molecular weight of 1140.
    Example 10
    The procedure of Example 3 was repeated except that 300 g (2.50 mol) of styrene oxide was used instead of propylene oxide while maintaining the pressure at 0.15 MPa or less, and the reaction period was 15 hours. The hydroxyl value was 81.3 and the number average molecular weight was 1380. 306 g of phosphorus transparent and odorless polyoxystyrenediol were obtained.
    Example 11
    The procedure of Example 3 was repeated except that 13.0 g (217 mmol) of ethylenediamine was used instead of dipropylene glycol to obtain 200 g of transparent, odorless polyoxypropylene tetraol having a hydroxyl value of 247 and a number average molecular weight of 910.
    Example 12
    Using 18.7 g (217 mmol) of piperazine instead of dipropylene glycol and repeating the procedure of Example 3 except that the reaction period was 8 hours, transparent and odorless polyoxy having a hydroxyl value of 117 and a number average molecular weight of 960. 211 g of propylenediol were obtained.
    Example 13
    The procedure of Example 3 was repeated, except that 15.4 g (217 mmol) of pyrrolidine was used instead of dipropylene glycol, and the reaction period was changed to 10 hours. A transparent, odorless poly having a hydroxyl value of 59.7 and a number average molecular weight of 940 206 g of oxypropylene monool were obtained.
    Hereinafter, the manufacturing method of the 1, 2- deoxyethane derivative as a 4th aspect of this invention is demonstrated.
    Example 14
    Into a 100 ml flask, 0.595 g (1.00 mmol) of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide and 14.3 g (105 mmol) of phenyl acetate were accurately weighed and heated to 90 ° C. 15.0 g (100 mmol) of phenylglycidyl ether was added dropwise to the mixture over 10 minutes. After the dropwise addition, the mixture was stirred at the same temperature for 5 hours and cooled to room temperature over about 10 minutes. A part of the reaction mixture was quantitatively analyzed by gas chromatography using 1,3,5-trichlorobenzene as an internal standard, and thus the consumed phenylglycidyl ether was almost completely consumed, and the desired acetic acid 1,3 was used. -Diphenoxy-2-propyl was formed in a yield of 98% based on phenylglycidyl ether. In brief, the reaction proceeded almost quantitatively.
    Direct column chromatography on the reaction mixture afforded 27.2 g of acetic acid 1,3-diphenoxy-2-propyl as a colorless liquid, and all the analytical data obtained were the same as for the reference standard. The catalytic activity of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide (molar amount of desired product per mole of catalyst in unit time (TON / h); hereafter the same definition is used) is 20TON / h Surprisingly about 13 times, 6 times or 7 times larger than that given by the respective N-methylimidazole, tetrabutylammonium chloride or potassium tert-butoxide in Comparative Examples 3, 4 or 5. Thus, phenylglycidyl ether and phenyl acetate reacted to produce acetic acid 1,3-diphenoxy-2-propyl, i.e. 1,2-dioxyethane derivatives, with remarkably high catalytic activity and high yield.
    Comparative Example 2
    The procedure of Example 14 was repeated except that tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide was not used. The yield of acetic acid 1,3-diphenoxy-2-propyl was 1%.
    Comparative Example 3
    The procedure of Example 14 was repeated except that equimolar amounts of N-methylimidazole were used in place of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide. The yield of acetic acid 1,3-diphenoxy-2-propyl was 8%, and the catalytic activity was as low as 1.5TON / h.
    Comparative Example 4
    The procedure of Example 14 was repeated except that equimolar amount of tetrabutylammonium chloride was used in place of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide. The yield of acetic acid 1,3-diphenoxy-2-propyl was 18% and the catalytic activity was as low as 3.6TON / h.
    Comparative Example 5
    The procedure of Example 14 was repeated except that equimolar amounts of potassium tert-butoxide were used in place of tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide. The yield of acetic acid 1,3-diphenoxy-2-propyl was 15% and the catalytic activity was as low as 3.0TON / h.
    Example 15
    In a 200 ml autoclave, ethyl acetate (37.0 g, 420 mmol) and tris [tris (dimethylamino) phosphoranylideneamino] phosphine sulfide (0.595 g, 1.00 mmol) were accurately weighed and warmed to 100 ° C. While 23.2 g (400 mmol) of propylene oxide was introduced intermittently, the reaction pressure was maintained at 0.4 MPa, and the system was heated at the same temperature for 13 hours. The mixture was then cooled to ambient temperature over about 30 minutes. Part of the reaction mixture was quantitatively analyzed by gas chromatography to show that the desired 2-acetoxy-1-ethoxypropane was formed in a yield of 90%. After distillation of the reaction mixture, 47.3 g of 2-acetoxy-1-ethoxypropane was obtained.
    Example 16
    The procedure of Example 15 was repeated except that equimolar amount of methyl benzoate was used instead of ethyl acetate and equimolar amount of ethylene oxide was used instead of propylene oxide. The yield of target benzoic acid 2-methoxyethyl was 89%.
    Example 17
    The procedure of Example 14 was repeated except that 1/2 molar amount of 2,2-bis (4-glycidyloxyphenyl) propane was used instead of phenylglycidyl ether. The yield of the target 2,2-bis [4- (2-acetoxy-3-phenoxypropoxy) phenyl] propane was 92%.
    Example 18
    The procedure of Example 14 was repeated except that equimolar amount of benzoate was used in place of phenyl acetate and equimolar amount of 4-phenoxyphenylglycidyl ether was used instead of phenylglycidyl ether. The yield of target benzoic acid 1-phenoxy-3- (4-phenoxyphenoxy) -2-propyl was 99%.
    Example 19
    The procedure of Example 14 was repeated except that equimolar amount of 5-methoxypentanoic acid 4-methoxyphenyl was used instead of phenyl acetate, and equimolar amount of glycidyl acetate was used instead of phenylglycidyl ether. The yield of the target 5-methoxypentanoic acid 1-acetoxy-3- (4-methoxyphenoxy) -2-propyl was 92%.
    Example 20
    The procedure of Example 15 was repeated except that equimolar amounts of methyl 4-phenoxybenzoate were used instead of ethyl acetate. The yield of the desired 4-phenoxybenzoic acid 1-methoxy-2-propyl was 84%.
    Example 21
    The procedure of Example 14 was repeated except that equimolar amount of acetic anhydride was used instead of phenyl acetate, equimolar amount of styrene oxide was used instead of phenylglycidyl ether, and the reaction temperature was 85 ° C. The yield of target 1,2- diacetoxyethylbenzene was 97%.
    Example 22
    The procedure of Example 14 was repeated except that equimolar amount of benzoic anhydride was used in place of phenyl acetate, equimolar amount of 4-methoxycarbonyl styrene oxide was used instead of phenylglycidyl ether, and the reaction temperature was 85 ° C. The yield of target 1- (1,2-dibenzoyloxyethyl) -4-methoxycarbonylbenzene was 94%.
    Example 23
    The procedure of Example 14 was repeated except that equimolar amount of dimethyl carbonate was used in place of phenyl acetate, and 4-methoxystyrene oxide was used in place of phenylglycidyl ether. The yield of target 1- (1-methoxy-2-methoxycarbonyloxyethyl) -4-methoxybenzene was 82%.
    Example 24
    The procedure of Example 14 was repeated except that equimolar amounts of diphenyl carbonate were used instead of phenyl acetate. The yield of the intended 1,3-diphenoxy-2-phenoxycarbonyloxypropane was 86%.
    Example 25
    The procedure of Example 14 was repeated except that equimolar amounts of 2-methoxyethyl4-methoxyphenylcarbonate were used instead of phenyl acetate. The yield of target 1-phenoxy-3- (4-methoxyphenoxy) -2- (2-methoxyethoxycarbonyloxy) propane was 96%.
    Example 26
    The procedure of Example 14 was repeated except that equimolar amounts of phenol were used instead of phenyl acetate. The yield of target 1,3-diphenoxy-2-propanol was 99%.
    Example 27
    The procedure of Example 14 was repeated except that 1/2 molar amount of 2,2-bis (4-hydroxyphenyl) propane was used instead of phenyl acetate. The yield of the target 2,2-bis [4- (2-hydroxy-3-phenoxypropoxy) phenyl] propane was 95%.
    Example 28
    The procedure of Example 14 was repeated except that equimolar amounts of 4-chlorophenol were used instead of phenyl acetate. The yield of target 1- (4-chlorophenoxy) -3-phenoxy-2-propanol was 97%.
    Example 29
    The procedure of Example 14 was repeated except that equimolar amounts of 3-phenoxyphenol were used instead of phenyl acetate. The yield of target 1- (3-phenoxyphenoxy) -3-phenoxy-2-propanol was 93%.
    Phosphine sulfide represented by the general formula (1) of the present invention is a novel compound which is basic and soluble in an organic solvent, which exhibits catalytic activity as a basic compound without any problems during manufacture or handling.
    According to the present invention, phosphine sulfide having such a property can be conveniently prepared.
    According to the present invention, poly (alkylene oxide) can be efficiently produced by polymerizing alkylene oxides without any treatment before polymerization and no residual amine odor. In addition, 1,2-dioxyethane derivatives can be efficiently produced by reacting an epoxy compound with a carboxylate, carboxylic anhydride, carbonate or phenol compound.
    权利要求:
    Claims (13)
    [1" claim-type="Currently amended] Formula (1):

    (Wherein R may be the same or different and each represents a hydrocarbon group having 1 to 10 carbon atoms);
    [2" claim-type="Currently amended] The phosphine sulfide according to claim 1, wherein R in General Formula (1) is a methyl group.
    [3" claim-type="Currently amended] In the method for producing phosphine sulfide represented by the general formula (1) of claim 1, 1 mole of thiophosphoryl chloride and the general formula (2):

    Wherein R is the same or different and each represents a hydrocarbon group having 1 to 10 carbon atoms.
    [4" claim-type="Currently amended] The method for producing phosphine sulfide according to claim 3, wherein R in General Formula (2) is a methyl group.
    [5" claim-type="Currently amended] In the method for producing a poly (alkylene oxide), an organic compound having a phosphine sulfide represented by the general formula (1) of claim 1 or the phosphine sulfide and water and a partial structure of -OH or -NH- A method for producing a poly (alkylene oxide), comprising the step of polymerizing an alkylene oxide in the presence of an active hydrogen compound selected from:
    [6" claim-type="Currently amended] The method for preparing poly (alkylene oxide) according to claim 5, wherein the alkylene oxide is selected from the group consisting of ethylene oxide, propylene oxide, 1,2-butylene oxide and styrene oxide.
    [7" claim-type="Currently amended] Formula (3), (4), (5) or (6):


    In the method for producing a 1,2-dioxyethane derivative having a partial structure represented by (wherein, the carbon atom C- or -C attached to a carbonyl group or an oxygen atom belongs to an aliphatic, alicyclic or aromatic hydrocarbon), 1,2-di, comprising the step of reacting an epoxy compound with a carboxylate, a carboxylic anhydride, a carbonate or a phenol compound in the presence of a phosphine sulfide represented by the general formula (1) according to item 1 Method for producing oxyethane derivative.
    [8" claim-type="Currently amended] The method of claim 7, wherein the epoxy compound is (a) an aliphatic or aromatic epoxy compound consisting of an oxygen atom of the epoxy group and carbon and hydrogen atoms; (b) aliphatic or aromatic epoxy compounds having ether bonds; Or (c) an aliphatic or aromatic epoxy compound having an ester bond.
    [9" claim-type="Currently amended] 8. The method of claim 7, wherein the carboxylate is (a) an aliphatic or aromatic carboxylate consisting of an oxygen atom of an ester bond and a carbon and hydrogen atom; Or (b) an aliphatic or aromatic carboxylate having an ether bond.
    [10" claim-type="Currently amended] 8. The process for producing 1,2-dioxyethane derivatives according to claim 7, wherein the carboxylic anhydride is an aliphatic or aromatic carboxylic anhydride consisting of an oxygen atom of an anhydrous carboxylic acid group and a carbon and a hydrogen atom.
    [11" claim-type="Currently amended] The method of claim 7, wherein the carbonate is (a) an aliphatic or aromatic carbonate consisting of oxygen atoms of the carbonate group and carbon and hydrogen atoms; Or (b) an aliphatic or aromatic carbonate having an ether bond.
    [12" claim-type="Currently amended] 8. The phenolic compound according to claim 7, wherein the phenolic compound comprises: (a) a phenolic compound consisting of an oxygen atom of a phenolic hydroxyl group and a carbon and hydrogen atom; (b) halogenated phenolic compounds; Or (c) a phenolic compound having an ether bond.
    [13" claim-type="Currently amended] The process for producing 1,2-dioxyethane derivatives according to any one of claims 5 to 12, wherein R in the general formula (1) is a methyl group.
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    同族专利:
    公开号 | 公开日
    DE69907081T2|2004-03-04|
    KR100325840B1|2002-03-07|
    EP0972776A1|2000-01-19|
    ID25965A|2000-11-16|
    CN1262276A|2000-08-09|
    SG80048A1|2001-04-17|
    EP0972776B1|2003-04-23|
    CN1190441C|2005-02-23|
    DE69907081D1|2003-05-28|
    TW568915B|2004-01-01|
    US6153794A|2000-11-28|
    MY115637A|2003-08-30|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1998-07-15|Priority to JP20085898
    1998-07-15|Priority to JP1998-200858
    1998-12-17|Priority to JP35951798
    1998-12-17|Priority to JP1998-359517
    1999-07-15|Application filed by 사토 아키오, 미쯔이카가쿠 가부시기가이샤
    2000-02-25|Publication of KR20000011756A
    2002-03-07|Application granted
    2002-03-07|Publication of KR100325840B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP20085898|1998-07-15|
    JP1998-200858|1998-07-15|
    JP35951798|1998-12-17|
    JP1998-359517|1998-12-17|
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