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&&3-Bromopropionyl chloride，
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Copyright (C)
DXY All Rights Reserved.Process for the preparation of 2,3-dibromopropionyl chloride
United States Patent 5344977
An improved process for the preparation of 2,3-dibromopropionyl chloride, which comprises brominating acrylic acid, adding iron powder or an iron salt to the resultant melt, chlorinating the dibromopropionic acid obtained, and removing the volatile components. The 2,3-dibromopropionyl chloride is obtained in high yield and purity and is an intermediate for synthesising in particular reactive dyes.
Inventors:
Arquint, Alfons (Basel, CH)
Leupin, Peter (Basel, CH)
Application Number:
Publication Date:
09/06/1994
Filing Date:
01/22/1993
Export Citation:
Ciba-Geigy Corporation (Ardsley, NY)
Primary Class:
Other Classes:
International Classes:
B01J23/745; B01J27/053; B01J27/128; B01J27/25; C07B61/00; C07C51/363; C07C51/58; C07C51/60; C07C53/50; (IPC1-7): C07C53/19; C07C53/42; C07C53/50
Field of Search:
562/861, 562/862, 562/863, 562/864
View Patent Images:
&&&&&&PDF help
US Patent References:
4994562Lehmann534/5994990599Mausezahl et al.534/6344917705Mausezahl et al.534/6364892870Lee514/2114885360Scheibli534/6424855410Oxenius et al.534/5914801694Scheibli et al.534/6374528146Bockmann et al.562/86.34065446Bien et al.534/5824039523Hegar534/6183364259Scigliano et al.260/5441805162Britton562/862
Foreign References:
JP0163342October, 1982562/862JPSA
Other References:
Streitwieser & Heathcock, "Introduction to Organic Chemistry", Macmillan Publishing Co., New York (1976), pp. 444 & 581.
Asinger et al., Journal fur Praktische Chemie, 314, pp. 80-86 (1972).
Pizey, "Synthetic Reagents," vol. 1, pp. 333-335 (1974).
R. S. Davidson et al., J. Soc. Dyers Colour, vol. 104(2), pp. 86-93 (1988).
Primary Examiner:
Dees, Jose G.
Assistant Examiner:
Frazier, Barbara S.
Attorney, Agent or Firm:
Mansfield, Kevin T.
Parent Case Data:
This application is a continuation of
application Ser. No. 07/699,543, filed May 14, 1991, now
abandoned.
What is claimed is:
1. A process for the preparation of 2,3-dibromopropionyl chloride, in one reactor without isolation of intermediate compounds, which consists essentially of the following sequence of steps:
a) brominating acrylic acid with liquid bromine in the temperature range from 20° to 70° C.,
b) adding iron powder or an iron salt selected from the group consisting of iron(III) chloride, iron(II) chloride, iron(II) iodide, iron(II) nitrate, iron(III) bromide, iron(II) oxide, iron(III) oxide, iron(II) hydroxide, iron(III) hydroxide and iron(II) sulfate to the resultant melt,
c) chlorinating the dibromopropionic acid obtained to 2,3-dibromopropionyl chloride by adding 5 to 25% excess thionyl chloride thereto uniformly over a period of 3 to 10 hours in the temperature range from 55° to 75° C., substantially in the absence of a solvent, and
d) removing the volatile components.
2. A process according to claim 1, wherein the iron salt in step b) is iron(III) chloride.
3. A process according to claim 1, wherein 0.01 to 2.0 mol % of iron powder or an iron salt is added in step b), based on the acrylic acid.
Description:
The present invention relates to an improved single step process for the preparation of 2,3-dibromopropionyl chloride, which comprises the steps of:
a) brominating acrylic acid,
b) adding iron powder or an iron salt to the resultant melt,
c) chlorinating the dibromopropionic acid obtained to 2,3-dibromopropionyl chloride, and
d) removing the volatile components. The 2,3-dibromopropionyl chloride obtained by the process of this invention is obtained in high yield (over 97%) and high purity (more than 98%). 2,3-Dibromopropionyl chloride is, as reactive component, an important intermediate for the synthesis of reactive dyes. The inventive feature consists in adding iron powder or an iron salt to the resultant melt in accordance with step b) above. Specifically, the reaction is carried out as follows:
a) Acrylic acid (CH2 ?CH--COOH) is brominated. Bromination is effected by charging a small excess (.about.1%) of the brominating agent, preferably liquid bromine, to the reactor and adding acrylic acid dropwise in the temperature range from 20° to 70° C.
b) As soon as a melt has formed and all the acrylic acid has been added, iron powder or an iron salt, conveniently in the form of a 40% aqueous solution, is added in the temperature range from 20°-70° C. to this melt. It is advantageous to add 0.01 to 2.0 mol %, preferably 0.1 to 0.3 mol %, most preferably 0.2 mol %, of iron powder or iron salt (based on the acrylic acid). Particularly suitable iron salts are: iron(III) chloride, iron(II) chloride, iron(II) iodide, iron(II) nitrate, iron(III) bromide, iron(II) oxide, iron(III) oxide, iron(II) hydroxide, iron(III) hydroxide and iron(II) sulfate. The preferred iron salt is iron(Ill) chloride. The addition of the iron powder or iron salt is followed by the step of
c) chlorinating the dibromopropionic acid (CH2.Br--CH.Br--COOH) to 2,3-dibromopropionyl chloride (CH2.Br--CH.Br--COCl) by adding the chlorinating agent, preferably thionyl chloride, over 3 to 10 hours uniformly in the temperature range from ca. 55° to 75° C., preferably at 65° C., with stinting, to the melt (conveniently using an excess of 1-30%, preferably 5-25% and, most preferably, 15-22% of chlorinating agent), to give a reaction mass which contains more than 95% of 2,3-dibromopropionyl chloride, and from which
d) the volatile components, in particular HCl and SO2 and excess thionyl chloride, are removed over the course of 1-2 hours, conveniently by vacuum distillation, for example applying a vacuum of up to 25 mbar. The invention is illustrated by the following non-limitative Examples.
EXAMPLE 1 The reactor is charged with 224 g of bromine at 15°-20° C. With stirring, 100 g of acrylic acid are added uniformly over 8 hours. Simultaneously the temperature rises and the reaction mixture refluxes. After stirring for 30 minutes at 64°-66° C., a melt of 2,3-dibromopropionic acid is obtained. To this melt are then added 1.1 g of iron(III) chloride solution (40% in water). With stirring, 191 g of thionyl chloride (15% excess) are added uniformly to the melt at 65° C. over 5 hours. Stirring is continued for ca. 1 hour at 65° C. until the evolution of gas has ceased. The crude reaction mass so obtained has a purity of 93-95% and the volatile components are removed by evacuating at 65° C. to 25 mbar and degassing for ca. 11/2 hours, to give 344 g of 2,3-dibromopropionyl chloride (98% of theory, based on acrylic acid) in a purity of 98-99%. EXAMPLE 2 (Comparison Example) The reactor is charged with 224 g of bromine at 15°-20° C. With stirring, 100 g of acrylic acid are added uniformly over 8 hours. Simultaneously the temperature rises and the reaction mixture refluxes. After stirring for 30 minutes at 64°-66° C., a melt of 2,3-dibromopropionic acid is obtained. With stirring, 280 g of thionyl chloride (75% excess) are added to the melt at 65° C. over 4-6 hours. Stirring is continued for 18-22 hours at reflux at increasing temperature to 85°-90° C. until the evolution of gas has ceased. The crude reaction mass so obtained has a purity of 75-80%. The excess thionyl chloride is removed by distillation at 60°-70° C. and 100-200 mbar over ca. 2 hours. To remove the volatile components completely, the reaction mass is evacuated at 65° C. to 25 mbar and degassed for 1-2 hours, giving 341 g of 2,3-dibromopropionyl chloride (95% of theory, based on acrylic acid) in a purity of 94-96%.
______________________________________
Composition of the final product in HPLC (% by weight) Ex. 1 with Ex. 2 without iron(III)
iron(III) Designation
______________________________________
2,3-dibromopropionyl chloride98-99%
94-96%(main component)2-bromoacryloyl chloride&0.2%
2-3%(secondary component)
______________________________________
& 2004-. All rights reserved.细胞库/细胞培养
ELISA试剂盒
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&&3-Bromopropionyl chloride，
3-Bromopropionyl chloride，
&丁香通采购保障计划，让您的采购更放心。
供应商信息
商家诚信度：
成立时间：2014年
入驻丁香通年限：3年
商家等级：金牌客户
产品信息完整度：72%
联系人：付经理
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