• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    1365952 Diesteramides SNAM PROGETTI SpA 12 Oct 1971 [13 Oct 1970 (2)] 47521/71 Heading C2C [Also in Division C3] Diesteramides having the general formula wherein each R<SP>4</SP> is a hydrocarbon radical selected from alkyl radicals having from 1 to 8 carbon atoms, aryl radicals having from 6 to 10 carbon atoms, and cycloalkyl radicals having from 4 to 10 carbon atoms with the proviso that, when one radical R<SP>4</SP> is an aryl radical, the other radical R<SP>4</SP> is not an acyclic alkyl radical; and each of A and B, which may be the same or different, is an unsubstitued or substituted aliphatic or aromatic, divalent radical having from 2 to 30 carbon atoms, are prepared by reacting a dicarboxylic acid ester of the formula with a diamine of the formula there being present during the reaction more than two moles of the dicarboxylic acid ester for each mole of diamine. The diesteramides prepared according to the invention may be used in the preparation of polyesteramides.
    公开号:SU1069623A3
    申请号:SU711703305
    申请日:1971-10-11
    公开日:1984-01-23
    发明作者:Кичери Луиджи；Ди Григорио Франческо；Пяатоне Эдуардо
    申请人:Снам Прогетти С.П.А. (Фирма)；
    IPC主号:
    专利说明:

    about: with about:
    tsD
    OO
    It is a product from a solution that was previously transparent. Heating was continued for another 6.5 hours, after which the mixture was filtered at 65 ° C, and the filter cake was washed with toluene (.2200, heated to 65 ° C, and boiling methyl alcohol (2200 CM.I. After drying, in a drying oven 8 g of the desired product are obtained (80% of the theoretical yield with respect to the initial di-amine). T.SH .. 202-204®С.
    Example 4: A4-di-n, k- (p-Metoxicop6o-nylbenzoyl-aminomethyl-benzrl.
    960 cm3 anhydrous toluene ,. 210 cm of anhydrous methyl alcohol, 4.0.8 g (0.3 mol di-α- (aminomethyl J-benzol a and 407, I. g dimethyl terephthalate (2.1 mol mol) is placed in a three-liter three-necked flask equipped with a stirrer, a reflux condenser and a device for introducing an inert gas. The mixture is kept for some time at 67-70 ° C, and then 65f2 cm (0.83 M) of a solution of lithium methylate in methyl alcohol is added to it. After 70 minutes, precipitation is observed , the reaction was considered complete after h. The product was separated by hot filtration, washed with toluene to remove dimethyl phatalate, and then water with BCO C-2 to remove the catalyst. The yield of the product, which is a white powder, is 112 g, mp 213 sec. The content of amino groups is 28.2 meq.
    Elemental analysis.
    Calculated,%: C 67.80, H 5.20, N 6.10.
     Determined,%: C 68.00; H 5.30; N 6.20.
    Example 5: 1,4-di-DJ. N- | n-Metoxycarbonylbenzoyl-aminomethyl 3-cyclohexane.
    407.4 g of dimethyl terephthalate and .42.6 g of 1,4-di- {amInomethyl) -cyclohexane are dissolved in 60 cm in anhydrous toluene and 235 cm in anhydrous methyl alcohol in the flask described in the pre-example. The mixture is heated at 67-70 ° C, and then a 1.21 M solution of lithium 1-ethylate is added. The reaction ends after 9 hours.
    The precipitated product is filtered and heated on a Buchner funnel, washed with one liter of hot toluene, and then with hot water to remove the catalyst.
    The product in the form of white peas is obtained with a yield of 79% in relation to the starting diamine. M.p. 278c, the content of amino groups
    41.3 meq / kg.
    Elemental analysis. Calculated,%: C, 66.90) H, 6.44, and 6.01,
    Determined,%: C, 66.80, 6.70 / N, 6.30. Example 6. l, 2-di-fN, N- (rt-Metoxycarbonyl) -1 Mino-ethane.
    In a flask with a stirrer with a connecting device for supplying nitrogen, a column for. distilling off with a thermometer introduced into the reathionic mixture, see &amp; 1,2-dia1 "1Noethane with 233 g of dimethylterephthalate dissolved in 650 cm of boiling toluene and 170 cm of boiling methyl alcohol, then 14.4 cm 1 are added to the reaction mixture , 91 m. Solution of lithium methylate in methyl alcohol. The process ends in 5 hours. . -. The product is separated by hot filtration with a vichner funnel, washed with HOO cm hot H70 ° C toluene, then 500 C cold water to remove the catalyst. The result is 25 g of a white product, which is recrystallized from dimethylformamide.
    M.p. product, the content of amino groups of 28.6 meq / kg.
    Elemental analysis.
    Calculated,%: C 62.6; H 5.4; H 7.3.
    Determined,%: C 62,7; H 5.4, N 7.5,
    Example 7. 1,12-di- (H, H-Carbomethoxy-octanoyl-amino) dodecane. In a flask equipped as described in Example 5, a solution of 40 g of 1,12-dodecandiamine in 650 cm of anhydrous toluene and 158 cm of anhydrous methyl alcohol. After adding 260 g of azelamine dimethyl ether, the mixture is heated (70 ° C until a homogeneous solution is obtained. Then 14.4 cm 3 (1.91 M) of a solution of lithium methylate in methyl
    alcohol. After 9 h, the reaction mixture is cooled and the product is flashed using a Bjox Hepa funnel. The filter cake is washed (without heating / ethyl ether, taken in an amount of 500 cm.
    The resulting product 181 g) is recrystallized from methyl alcohol at a volume ratio of 1/50,
    The yield of the product, which is a white powder, is 71% relative to the starting amine, and its amino group content is 44.6 meq / kg.
    Elemental analysis.
    Calculated,%: C 67, b; H 10.57; H 4.93.
    (
    It is determined I: C 67.8, - H 10.7 / N 5.3.
    Example 8.1, 7-di- | Gk, N-In -Methoxycarbonylbenzoyl) amino D-heptane.
    In a flask equipped as described in Example 5, 26 g of 1.7-heptanediamine are dissolved in 780 cm of anhydrous toluene and 220 cm of methyl alcohol, and then 233 g of dimethyl terephthalate is added. After a homogeneous solution is obtained, a 1.91 M solution of lithium methoxide is added to the mixture. After an hour, the diamino ether begins to form and fade. The reaction continues for 4.5 hours. with stirring. Thereafter, the reaction mixture is cooled at room temperature and 2 L of chloroform is added to dissolve the residual dimethyl tereft-alate. The product which has separated out is filtered, rolled and dried under high vacuum. This product is then a white powder.
    (yield 93.D), washed with boiling chloroform, then with cold methyl alcohol to remove traces of catalyst. The resulting diamine. ether (yield 57%. in relation to the original diamine) has so pl. 220 ° C.
    Elemental analysis.
    Calculated,%: C 66.10; H 6.61, N 6.17.
    C HjjjN20
    Determined%: C 66.50, H 7.0, N 6.53 ..,
    P R.im a p 9. l, 5-di-fN, N - (p -Methoxycarbonylbenzoyl) -amino} pentane.
    Under the conditions of the previous example, 24.5 g of 1,5-pentamethylenediamine and 233 g of dimethyl terephthalate are dissolved in a mixture of 780 cm 3 of anhydrous toluene and 220 cm of methyl alcohol when heated. After complete dissolution is observed and the contents of the flask become clear, 17.3 cm (1.91 MJ dimethyl methylate solution in methyl alcohol is added to the reaction mixture. After 65 minutes, a precipitate begins to form. The reaction is continued while stirring 270 minutes, the diamine ester is filtered off using a hot ovane filter using a Buchner funnel, and washed with 1 liter of hot chloroform to remove excess dimethyl terephthalate. After dichlorization, the product is filtered and filtered with hot methyl alcohol for removing traces of inorganic salt
    The product, Zedstavl cadium, a white solid, is obtained in the amount of 61 g (59% yield with respect to the starting iodiamine). It is recrystallized from dimethylformamide, in which it is dissolved under EO-SOO S. So pl. product. The amino group content is 29.3 meq / kg, the elemental analysis of the product (jiljjN O) coincides with the calculated data.
    Example 10. "-di- (n, N-Methoxycarbonyloxanoyl Naminomethylbenzene.
    In a flask equipped as described in Example B, 28 g of metaphenylene dimethylenediamine and .250 g of yello-new dimethyl ether are dissolved in a mixture of 390 cm of anhydrous toluene by heating.
    , 110 cm of methyl alcohol. Then, 17.3 cm (1.91 M) of a solution of lithium methylate in methyl alcohol is added. The process is carried out at 6-7-70 ° C for 300 minutes, then 1500 mixtures of heptane and ethyl ether (1: 1) are added to the reaction of CMecfc in order to precipitate the diamino ether. The resulting product is filtered, using funnel
    Buchner is washed several times with the same mixture of solvents and then with water to remove the catalyst. After drying, the product weighs 40 g. ITS so pl. 113 ° C.
    Elemental and “alis.
    Calculated,%: C 66.7; H 8.73; N 5.56.
    ..
    Determined,%: C 66.8; H 8.70; N 5.60.
    . Example 11. 1,12-di-Gk, n-t P-Butoxycarbonylbenzoyl) amino-drdecan.
    Under conditions similar to those described in the previous example,
    40 i: 1.12-dodecanediamine and 334 g of dibutyl terephthalate i i. 650 cm of anhydrous n-heptane and 170 cm H-butyl alcohol. The reaction mixture is heated to 95 ° C and when it occurs.
    the complete dissolution and the reaction mixture become transparent; 14.5 cm 3 (1.17 M) of lithium n-butylate solution in methyl alcohol is added to it. Aminoether falls in
    sediment after 70 min. The product is filtered off, washed with acetone, recrystallized from boiling M-Utilized alcohol.
    The resulting product, which is a white solid, has m.p., leb-ieS C, amino group content of 29.4 meq / kg.
    Elemental analysis.
    Calculated,%: C 71.0; H 8.6; F 4.6.
    Defined, %; C, 71.3; H 8.7, 4.6.
    EXAMPLE 12 Dibutyl terephthalate 1DBT1 is reacted with dodecamethylenediamine (DMDA in a mixture of xylene and butyl alcohol. These substances, including a mixture of solvents and added sodium methyl, are used in the following amounts: 155, b (0.6 mol DVT, g (0.1 mol, DMD, g Methyl V0.0l mol sodium, g 0.54 Xylol / bug tilovy alcohol. p5 / 25, - ml 400 The reaction is carried out in a one-liter three-neck flask equipped with a reflux cooler, an agitator with nitrogen supply. The flask is filled with nitrogen, DBT is dissolved in the solvent mixture, the reaction with eu; heat, then the catalyst and diamine are added, and the reaction is continued at boiling point of the reaction mixture for 7 hours. To facilitate filtering, add 1 l of acetone to the reaction mixture. The filtered product is washed first with acetone and then with ethyl ether. The product processed by TaifHM is dried at 70 ° C in a drying oven under reduced pressure, etc. The product obtained. - 20 g of product are obtained, which corresponds to 33% of the theoretical yield. Elemental analysis. Calculated,%: C 71.05; H 8.557 N 4.60: Calculated,%: C, 70.8; H 8.55; N 4.65. Example 13: 1.12-di-k, k. - (p-Me, toxicarbonylbenzoyl) -amino-dodecanediamine. In a three-liter autoclave with a stirrer / providing vigorous stirring, a88 g (2 mol of dimethyl terephthalate, 80 g 1, a2-dod eecanediamine, 1280 cm of unvoiced toluene, 320 cm of absolute methyl alcohol and 37.6 cm3 of 1.41 M) of methane l ata lithium in methyl alcohol. The autoclave has an inert atmosphere. After the exclusion of these substances in the autoclave, it is filled with nitrogen with a succession of nitrogen with vacuum evacuation. Then the reaction mixture is heated to 130 ° C. The pressure in the autoclave is raised to about 9 kg / s. The reaction ends after 2 hours. The reaction mixture was removed from the autoclave and filtered while hot (465 ° C). filter; The bath product is washed with hot toluene (and liquefied with alcohol ()). After drying in an oven, 190 g of product are obtained (yield 90.9% relative to the starting diamine /. mp. 203-205 С The content of minor groups is 55 meq / kg. The elemental analysis of the product is consistent with theoretical data. (Measure 14, 4,4 -Di-Gn, and - (H-Methoxycarbonylbenzoyl Namino-diphenyl ether. In a flask equipped as described in Example 4, at 67-70® e: 116.5 tons of dimethyl terephthalate are dissolved in a mixture of toluene and methyl alcohol (72:75 by volume). Then 10.8 g are added. sodium ethyl acetate and 20 g of 4,4-diaminodiphenyl ether. A gray, barely noticeable dispersion is obtained. By maintaining a nitrogen atmosphere in the flask, the reaction mixture is brought to a boil, which is maintained for 10 hours. After the end of the reaction, the mixture is treated in the cold state is hydrochloric acid, which is taken in stoichiometric amount with respect to the catalyst, while the stirring is continued for some time. The product is then filtered, washed several times with chloroform to remove excess dimethyl terephthalate, and then with methyl alcohol. The product, which is a white solid, is obtained with a yield of 33% (relative to the starting diamine). M.p. 341 ° C. Elemental analysis. Calculated,%: C 68.7 / H 4.5 j N5.3. Determined,%: C 6B, 2; H 4.6; N 5.2. The resulting d aminodiesters of the general formula 1, when heated with flt, w-alkylene glycols, form a polymer. polyamide esters of an ordered structure, I Preparation of a polyamino ether from N, N - (p-butoxycarbonylbenzoyl) -dodecamethylenediamine and 1.12-dodecane-. diol 12 N, t 12. 262 g (0.43 mol; N, N- (p-butoxycarbonylbenzoyl-dodecamethylenediamine amine, obtained according to example 1, is placed in a one-liter flask with a vacuum stirrer, inert gas injection device and column Vigre, B for one hour, the product is kept in vacuum to remove gases dissolved in it, and then in an inert atmosphere 217 g (1.075 mol), 1.12-dodecanediol and 0.43 cm (2 M) of tetrabutyl titanium solution are added in butyl alcohol. The flask is placed in a bath in which the temperature is maintained, and with constant stirring in the flask I maintain Inert atmosphere. The reaction mixture is kept under the specified conditions for 3 hours, and then another 3 hours and 25 minutes, at 220 C. As a result of this treatment, 77 cm of butyl alcohol are removed from the mixture. The aad connector is a device for distillation in vacuum and for 1 hour 40 minutes the pressure in the tank is reduced from 760 to 0.5 4 MHg, while the temperature of the bath is increased from 220 to 2 ° C. Then, at a flask pressure of 0.5 mm Hg. The heating temperature is increased to 270 ° C and after 55 minutes the polycondensation is completed. The polymer obtained is mostly colorless; its relative viscosity is 2.52 when measured in a phenol tetrachloroethane solution (50:50 at a concentration of 1 g / dl. From a polymer whose density is 1.16 and a single thread is obtained by a known method using a melt at 280 s and drawing the thread with using a pin heated to EO ° C and a plate heated to 150 ° C. The stretched thread is dyed using dyed dispersed orange dye 13, which is used with a large excess of 1100%) using ammonium sulfate-formic acid buffer solution with a pH of 5.5, pr m liquor ratio is 1: 100. , According to the saturation isotherm, it will determine the rate constant for coloring and the value of saturation. The thread, processed by various soba, has a trace mechanical characteristics and harakistiki dyeability. Raw thread Titer, denier 10.7 Strength, g / den 5.1 Relative. . elongation,% 15 Modulus, g / day 60 Modulus TV wet state,% 97 units in a dry condition,% 97 Paintability Cd, d2 / kg, from 15.3% КТ. 40.5 Thread treated by boiling in water. Current 20 min. Strength, g / day 4.5 Relative elongation,% 22 Module, g / day 40 Module in the wet state,% 100 Module in the dry state,% 100 Thread , processed by heating in an atmosphere of air for; 10 min, and then boiling in water for 30 min. Strength, g / den 4.6 Relative elongation,% 20 Module, g / den 42
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING DIAMOND DIETHERS of the general formula,
    R-0-C-A-C-NH-B-NH-C-A-C-0-R
    НН н н ff о о о where R - - Су - alkyl, · · *
    A is phenylene, di- (C ^.-C 4 -alkylene) cyclohexane or c4, w-C ^ -¾ is alkylene;
    ft-cP, iu-Cy -C ^ 2 -alkylene, sim-di- (Сш -С ^ -alkylene / benzene or a radical of the formula characterized in that the diamine of the general formula in 2 - in - nn 2 , where β has values are introduced into interaction with an excess of diester of the General formula
    R-0-C-A-C-0-R H II 0 0 where A and R have the indicated meanings, in a mixture of anhydrous solvents, one of which is an aromatic hydrocarbon such as toluene, and the other is lower aliphatic. alcohol, such as methanol, in the presence of alkali metal alcoholate catalysts, such as lithium or sodium methylate, at 67-130 ° C.
    yes so yes ye w ’’ II. II o about alkyl i ‘.
    di- (C-C 4 -dlk ^, and . - C g-8
    II
    Oh where R 'A -
    类似技术:
    公开号 | 公开日 | 专利标题
    SU1069623A3|1984-01-23|Process for preparing diamidodiesters
    US2163636A|1939-06-27|Process for preparing linear condensation polyamides
    JP3498132B2|2004-02-16|Tetraalloxyperylene-3,4,9,10-tetracarboxylic acid polyimide
    US2293388A|1942-08-18|Polyamides and their preparation
    Nakata et al.1997|Preparation of aromatic copolyamides containing regularly placed 1, 6‐hexamethylenediamine units
    DE1795541C2|1982-06-03|Poly- |, process for its preparation and its use
    US3304328A|1967-02-14|Preparation of acetoacetarylamides
    US2281576A|1942-05-05|Polyamides and process of making same
    DE69835075T2|2007-01-04|Process for the preparation of polybenzazole
    CH617447A5|1980-05-30|
    US2659713A|1953-11-17|Process for preparing linear polyamides
    US3637739A|1972-01-25|Tetrahydrotetraazaporphine dyestuffs
    US2416738A|1947-03-04|Process for preparation of nu-substituted amides of beta-keto-carboxylic acids
    US3775423A|1973-11-27|Phthalocyanine-type dyestuffs
    US4952668A|1990-08-28|Process for the production of polyethyleneterephthalate from dimethylterephthalate
    US3558565A|1971-01-26|Polyamides from oxadicarboxylic acids and diamines containing aromatic nucleus
    Kurihara et al.1967|Cyclopolycondensations. IV. Investigation of the polymerization mechanism of aromatic diaminodicarboxylic acid in polyphosphoric acid and the thermal stability of aromatic polyamide amino acids
    TWI744125B|2021-10-21|Method for manufacturing transparent polyamide copolymer
    JP3475754B2|2003-12-08|Novel polyimide precursor, polyimide and method for producing the same
    EP0643039A1|1995-03-15|Ultraviolet ray-absorbing aromatic compound and polymeric composition containing the same
    SU749858A1|1980-07-23|Method of preparing copolybenzimidazolobenzoxazoles
    Russo et al.1997|Direct synthesis of aromatic polyamides
    US3272858A|1966-09-13|Method of producing arylamino acid color couplers
    Bicak et al.1989|Synthesis of new polyamidoximes and their crosslinking by transition metal ions
    US3335176A|1967-08-08|Aminomethyl carboxy dibenzyl amines and preparation thereof
    同族专利:
    公开号 | 公开日
    LU64050A1|1972-04-21|
    HU167518B|1975-10-28|
    AU3444971A|1973-04-19|
    YU258071A|1981-04-30|
    NL173952B|1983-11-01|
    BE773738A|1972-01-31|
    NO136192B|1977-04-25|
    CS174167B2|1977-03-31|
    JPS5730097B2|1982-06-26|
    NL7114102A|1972-04-17|
    CH535203A|1973-03-31|
    DE2150808C3|1979-04-12|
    DE2150808A1|1972-04-20|
    NO136192C|1977-08-03|
    DK150981B|1987-10-05|
    YU36144B|1982-02-25|
    DK150981C|1988-02-22|
    FR2111288A5|1972-06-02|
    NL173952C|1984-04-02|
    CA991199A|1976-06-15|
    GB1365952A|1974-09-04|
    DE2150808B2|1978-08-10|
    JPS53149921A|1978-12-27|
    JPS5516132B1|1980-04-30|
    SE378809B|1975-09-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    GB1588526A|1976-07-21|1981-04-23|Anic Spa|Elastomeric copolyesteramides|
    FR2362180B1|1976-08-20|1979-07-06|Ato Chimie|
    IT1123574B|1979-09-10|1986-04-30|Anic Spa|PROCESS FOR THE PRODUCTION OF DIESTEREDIAMIDES|
    DE3003898A1|1980-02-02|1981-08-13|Dynamit Nobel Ag, 5210 Troisdorf|METHOD FOR ACYLATING AMINOCARBONIC ACIDS|
    JPS60160816U|1984-04-02|1985-10-25|
    JPS62180419U|1986-05-09|1987-11-16|
    IT1190137B|1986-06-20|1988-02-10|Eniricerche Spa|FIBER, POLYESTER AMID QUARRY AND PROCEDURE FOR ITS PREPARATION|
    US5852155A|1995-03-01|1998-12-22|General Electric Company|Compositions of polyesteramides|
    US5744068A|1996-01-24|1998-04-28|General Electric Company|Blends of polyphenylene ethers and polyesteramides|
    US5731389A|1996-04-24|1998-03-24|General Electric Company|Blends of polyesters and polyesteramides, optionally with polycarbonates|
    US8685431B2|2004-03-16|2014-04-01|Advanced Cardiovascular Systems, Inc.|Biologically absorbable coatings for implantable devices based on copolymers having ester bonds and methods for fabricating the same|
    US10040904B2|2013-08-16|2018-08-07|Dsm Ip Assets B.V.|Process for producing a thermoplastic polymer containing segments of a diamide|
    CN109956881A|2017-12-26|2019-07-02|上海凯赛生物技术研发中心有限公司|A kind of benzoyl pentanediamine and its preparation and application|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    IT3090070|1970-10-13|
    IT3090170|1970-10-13|
    [返回顶部]