• 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:
    1. METHOD OF OBTAINING ni-CHLOROUS RANATED CHLORFORMIATS of total K- (CH-0-C-C1) w I and C1 o where R is methyl, isopropyl, butyl, isobutyl, vinyl, CCIj, CBtj, where X is 2-C1, 4-CHO, cyclohexen-3-yl, 2-chloro ELN1, then 1-2, by reacting phosgene with an aldehyde of the general formula R (CHO), where the value of R and m is indicated, in the presence of a catalyst, characterized in that output and expansion of the range of target products, as the catalyst used compounds selected from the group: pyridine, N, N-dimethylaniline, N, N-dimethylaminopyridine, imidazole, tetramethylurea, tet abutylurea, tetra-ni KC1 + cryptofix
    公开号:SU1184441A3
    申请号:SU813285452
    申请日:1981-05-13
    公开日:1985-10-07
    发明作者:Каньон Ги；Пито Марк；Сене Жан-Пьер；Арне Олофсон Рой；Томас Мартц Джонатан
    申请人:Сосьете Насьональ Де Пудр Э Эксплозив (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to an improvement of the method for producing chlorinated chloroformates, including (new compounds that can be used chemically. The method is carried out as follows. Example 1. In a 500 ml capacity reactor equipped with a stirrer, a thermometer, a cooler with dry ice and dropping funnel, placed 44 g (1 mol) of freshly distilled acetaldeguide, 200 MP anhydrous carbon tetrachloride and 120 g (1.2 mol) of phosgene, 28.4 g (0.1 mol) added to the mixture maintained during 15 minutes tetra-n-butylmo The wine was brought to 40 ° C and the reaction was continued for 2 hours and 30 minutes. After removing the excess phosgene by degassing and dissolving by evaporation, 72 g of 1-chloroethyl chloroformate were obtained, distilled at 50% by weight. The product formula is as follows: C1 CH3-C-0-C-Cl H) b in the IR spectrum a band appears at 1780 cm corresponding to the double bond, while the NMR spectrum in deuterated chloroform with an internal standard of tetramethylsilane shows the appearance doublet 1.85 MD, corresponding proton (), and quadruplet at 6.44 ppm corresponding to the proton (b). Example 2. A glass reactor with a capacity of 3 l equipped with an anchor stirrer, a thermometer, a refrigerator with a temperature of -35 ° C and a submerged tube was injected with 1000 ml of water washed and dried over magnesium sulfate dichloromethane, 440 g (10 mol of crude anhydrous acetaldehyde , 179 g (1 mol) of hexamethylphosphorus triamide. The mixture is cooled to -5 s and 1107 g of gaseous phosgene are introduced with stirring for 6.5 h. Then the temperature of the reaction medium is adjusted to 35-40 C and maintained for 3 h. They stay for 412 nights at room temperature, for the excess phosgene is removed by passing nitrogen for 4.5 hours. The resulting mixture is distilled under a pressure of 150 mm Hg in a glass column (height 40 cm, diameter 3 cm, spiral nozzle 0.5 cm) and the fraction thus, 1020.4 g of p6-chloroethyl chloroformate is obtained, which corresponds to a yield of 71% with respect to the initial acetaldehyde. Analysis: IR spectrum (): 1780 cm, 4220i d; 1.2946. Example 3. A 500 ml glass reactor equipped with an anchor stirrer, thermometer and reflux condenser with acetone-dry ice mixture is introduced 1 00 ml of water washed and dried over magnesium sulfate dichloromethane, 44 g (1 mol) of crude anhydrous acetaldehyde, 7.9 g (0.1 mol) of freshly distilled pyridine. The mixture is cooled to (-5 ° C) (-10 ° C) and 120 g of phosgene is added over about 1 hour. Then, for an hour, slightly boil under reflux (temperature AO 45C). The insolubles were filtered under nitrogen and the filtrate was distilled under reduced pressure. Thus, 90 g (yield 63%) o-chloroethyl chloroformate (m.p., h 68 C / 150 mm Hg) are obtained. Example 4. A reactor with a capacity of 100 ml, equipped as above, was introduced with 21.5 g (0.25 mol) n-pentanal, 50 ml of carbon tetrachloride and 1.9 g (0.025 mol) of pyridine. To this mixture, cooled to -5 ° C, 30 g (0.3 mol) of phosgene is added over 30 minutes. The temperature is gradually brought to 40 ° C. After an hour at this temperature, the reaction mixture is degassed with nitrogen, filtered and distilled under reduced pressure. Obtain 28 g of about-chlorine-n-alkylchloride, yield of 60.5%, so Kip. 73 ° / 15 mmHg IR spectrum ():: 1790.cm -, p ;; 1.4377; d 1.1523. NMR (CDClI, TMS): CH 3 CH 2 CH 2 CH 2 CHO-C-C 1 C 1 o (a) —array at 0.92 ppm (ЗН) (b) - massif at 1.40 ppm (4H) (c) -massive mass at 2.05 ppm (2H) (d) - triplet at 6.30 ppm (1H) Example 5. The use of the apparatus and method of operation, identical to those specified in example 4, use the following starting materials: Acrolein (propenal) 28 g (0.5 mol) Pyridin3.95 g (0.05 mol Carbon tetrachloride 50 ml Phosgene 60 g (0.6 mol). 0-Chlorallyl chloroformate distilled off at 38 ° C under a pressure of 10 mm Hg. The resulting mass is 42 g, corresponding to a yield of 54%. IR spectrum (): 1780 cm; n, 1.4462; d4l, 2853. NMR spectrum: H (a) / n (c1, CH (d) -C OCOCl (a) (b), (c) - complex array at 5.2-6.5 ppm (3N), (d) - doublet at 6.71 ppm Example 6. Products used are as follows: Benzald guide 26.5 g (0.25 mol Pyridine 1.95 g (0.025 mo Phosgen 35 g (0.35 mol) Carbon tetrachloride 50 ml. Analogously to Example 4, 34.8 g (68%) of ui is chlorobenzyl chloroform and distilled at 70 ° C infrared spectrum (): 1770 cm-; p 1.5367; df 1.3017 NMR spectrum: H-HOSOC1 H-HC1, all protons have a chemical separation of 7-8 m. Example 7: Similar to Example 6, but benzaldehyde is replaced by 2-chlorobenzaldehyde. 25.1 g (yield 42%) of chloro- (2-chloro) -benzylchloroformate are obtained, 41 distilled at 85-88 0 under a pressure of 0.2 mm Hg. IR (C 0): 1780 p 1.5420; 1.4294. NMR spectrum: OOS1 all protons have a chemical shift of 7-8 ppm Example 8. In a 500 ml capacity reactor, 67 g (0.5 mol) of terephthalaldehyde, 3.95 g (0.05 mol) of pyridine and 100 ml of carbon tetrachloride are placed. Then, 120 g (1.2 mol) of phosgene are added. The mixture is then gradually brought up and held at this temperature for 3 hours. After degassing, filtering and removing the solvent, 133 g (yield 80%) of a colorless oil are obtained. The total chlorine content (in%) was calculated to be 42.7 g; found 40.02. IR spectrum (): 1780 cm NMR spectrum (CDCl ,, (a) C1-CO-0-CH-O (a) - singlet at 7.29 ppm (GH), (b) - singlet with 7.64 ppm (4H), Example 9. In a reactor with a capacity of 100 type, 11 g (0.25 mol) of acetaldehyde, 9.25 g (0.025 mol) of trioctylphosphine and 50 ml of carbon tetrachloride are placed. , 30 g (0.3 mol) of phosgene are added to the mixture. After heating for one hour at 35-40 ° C, the reaction mixture is degassed and distilled under reduced pressure (150 mm Hg). Thus, 9.1 is obtained g (25% yield) of tki-chloroethyl chloroformate distilled at 67-68 ° C / 150 mm Hg Example 10. This experiment relates to sex Students about chloroethyl formate by phosgenating acetaldehyde in the presence of 5 mol.% pyridine in a solvent medium. The method and apparatus are identical to example 4, The quantities of products used are the following: Acetaldehyde 11 g (0.25 mol Pyridine: 0.99 g (0.0125mo Phosgene 30 g (0.3 mol) Methylene chloride 50 ml. Thus, 25.6 g (yield 71.6%) of chloroethyl chloroformate distilled at 68 ° C / 150 mm Hg is obtained. Example 11. This experiment relates to the preparation of ei-chloroethyl chloroformate by phosgenating acetaldehyde in the presence of 5 mol. % pyridine without solvent. In a reactor with a capacity of 100 ml, analogously to Example 10, 22 g (0.5 mol) of acetaldehyde and 1.98 g (0.025 mol) of pyridine are placed at 0 C. At this temperature, 60 g (0.6 mol) of phosgene are introduced. The reaction mixture is brought to 30 ° C over 4 hours and held at this temperature for 1 hour. After removal of phosgene, 42.1 g (yield 59%) of chloro-ethyl chloroformate, distilled at a pressure of 150 mm Hg, is obtained. Example 12 28 g (0.25 mol of niclohexylcarboxaldehyde, 1.98 g (0.025 mol) of pyridine and 50 ml of carbon tetrachloride are placed in a reactor with a capacity of 100 ml. 30 g (0.3 mol) are introduced into this mixture). phosgene. The reaction medium is then adjusted to 35-40 ° C and kept at this temperature for 1 hour. After degassing, filtering and lengthening Under a pressure of the solvent, 46 g (yield 87%) of the expected chloroformate distilled at 90-93 ° C / 10 mm Hg 1.4738, d 1.1934, NMR spectrum (CDC1., TMS): (( fo-c-ci n (a) is an array at 1.15-2.2 ppm (11 H) {(b) is a doublet at 6.1 ppm (1H), Examples 13-17. These experiments are similar to those of Example 4, illustrating the effectiveness of different catalysts depending on temperature. Each of these experiments is carried out using the following chemicals: Acetaldehyde 4.4 g (0.1 mol) and Toluene 45 g Catalyst 0.01 mol Phosgene 12 g (0.12 mol) Results obtained depending on the temperature after the reaction proceeds for 3 h are presented in Table. 1, with the progress of the reaction or the absence of the reaction being evaluated by IR spectrophotometry. The lack of reaction indicates that the yield is less than 5%. Examples 18-26. Two series of experiments were carried out with catalysts for the synthesis of chloroethyl chloroformate. These series of experiments differ only in the reaction temperature and the solvent used (Table 2). When in a hermetically sealed tube with a capacity of 20 ml, made of glass and capable of withstanding pressure, 0.001 mol of catalyst, a magnetized stirrer bar and 5 ml of a solution of 2 mol / l acetaldehyde and 5 ml of a solution of 2 mol / l phosgene in carbon tetrachloride (series 1 ) or in chlorobenzene (series 2). The amount of catalyst is thus 10 mol. % relative to acetaldehyde. Then the tube is quickly hermetically sealed, placed in a thermostatic bath with a temperature of 40 C (series 1) or (series 2). The stirring is started with a magnetic stirrer, the reaction is allowed to proceed for 3 hours. After this period the tube is cooled to approximately, a sample is taken from the reaction medium, which is immediately analyzed using NM (TM.C standard). When the reaction is carried out under the hood, there is no loss of acetaldehyde, which is in one of the following four forms: Nd corresponds to the quad C CH (a) 0 rump at 9.7 ppm, the integration of which is a. HI, corresponds to the quad of CH 3 SOS P P P whose integration has the value b. C1 CH3-CH with JHc j. corresponds to a quadrant of a ruble at 4.9 MD, the integration of which has a value of c. Hj corresponds to a quad ruble at 5.85 ppm. CHz-CHd integration of which is set to d. The yields of oh-chloroethyl chloroformate obtained with each of the catalysts are determined using the formula: 100 (a + b + c + d). Example 27. In a Keller flask with a capacity of 50 ml, equipped with a magnetic
    Table I with a stirrer and an ascending condenser with a mixture of acetone and dry ice maintained at the addition of 1.30 g (0.01775 mol) of KC1, 0.40 g (0.00106 mol) of commercial .. cryptfix (222), produced by the firm Megsk, 12.5 g (0.125 mol) of phosgene and 2.2 g (0.05 mol) of acetaldehyde. The reaction mixture is stirred for 5 hours at room temperature (18-22s). After this period, the analysis of the medium by NMR shows that the OC yield of chloroethyl chloroformate is 96%, the residue consists almost exclusively of acetaldehyde, Example 28. 0.5 g of tetra- n-Hexipammonium bromide, 6.25 g of phosgene and 1.1 g of acetic acid, the mixture is stirred for 4 hours at room temperature (18: 20 ° C). At the end of this time, the NMR spectrum of the mixture is taken and it is observed that only ei-chloroethyl chloroformate is present in the mixture, or the yield is 100%.
    13 N, N-dimesh1aminopyridine
    14 K, N-dimeshtanilin
    15 Imidazole
    16 Tetra-n-butyl-urea product with phosgene
    SG
    C I
    C
    17 Dimethylformamide
    No Reaction
    reactions
    Reactions
    No Reaction
    reactions
    Reactions 45
    (CCl4,)
    75
    (chlorobenzene, 100 C)
    Note, (a) tetrabutylurea
    (b) tetramethylamine
    (c) Michler's ketone,
    table 2
    ten
    15
    45
    65
    65
    75
    权利要求:
    Claims (2)
    [1]
    1. METHOD FOR PRODUCING OO-CHLORINATED CHLOROFORMATES of the general formula
    R-CH-O-C-SG) ^ I II
    Cl 0 where R is methyl, isopropyl, butyl, isobutyl, vinyl, CC1 3 , CBg 3 , C 6 H 4 X, where X is 2-C1, 4-CHO, cyclohexen-3-yl, 2-chloroethyl, w = 1-2, the interaction of phosgene with an aldehyde of the general formula R (CHO) m , where the values of R and m are indicated above, in the presence of a catalyst, characterized in that, in order to increase the yield and expand the range of target products, compounds are used as catalyst selected from the group: pyridine, N, Ν-dimethylaniline, N, N-dimethylaminopyridine, imidazole, tetramethylurea, tetrabutylurea, tetra-n-butylammonium chloride - reaction product tetrabutylureas with phosgene, tri-n-butylbenzylammonium chloride, tetra-n-butylammonium chloride, trioctiphosphine, hexametiphosphotriamide, dimethylformamide, di (p-dimethipaminophenip) ketone, tetra-n-hexylfonamide | KC1 + 18-crown-6, quinoline, taken in an amount of 5-10 mol.%, At 20 100 ° C.
    [2]
    2. The method according to p. 1, characterized in that the reaction is carried out in a non-polar or weakly polar aprotic solvent - dichloromethane, carbon tetrachloride, chlorobenzene, or the reaction product itself.
    >
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    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    FR8010806A|FR2482587B1|1980-05-14|1980-05-14|
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