GB541375A - Improvements in and relating to the manufacture of cyanoacrylic acid esters - Google Patents

Improvements in and relating to the manufacture of cyanoacrylic acid esters

Info

Publication number
GB541375A
GB541375A GB913140A GB913140A GB541375A GB 541375 A GB541375 A GB 541375A GB 913140 A GB913140 A GB 913140A GB 913140 A GB913140 A GB 913140A GB 541375 A GB541375 A GB 541375A
Authority
GB
United Kingdom
Prior art keywords
esters
acid
acid esters
chloracrylic
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB913140A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB913140A priority Critical patent/GB541375A/en
Publication of GB541375A publication Critical patent/GB541375A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

541,375. Cyanacrylic acid esters. CRAWFORD, J. W. C., McLEISH, N., WOOD, T. K., and IMPERIAL CHEMICAL INDUSTRIES, Ltd. May 23, 1940, No. 9131. [Class 2 (iii)] Esters of #-cyanoacrylic acid are produced by re-acting esters of α-chloracrylic acid with an alkali or alkaline earth cyanide in the presence of water or a water-miscible solvent of the chloracrylic ester, at temperatures not greatly above atmospheric, such as 0-30‹C. The re-action mixture may be buffered to a weakly alkaline state for instance by means of a bicarbonate or borate, and an anti-polymerization catalyst such as hydroquinone or aniline may be added. When an alkaline earth cyanide is used it may be made in situ. The product may be treated by fractional distillation and cis and trans forms may be separated by fractionation. Examples are given.
GB913140A 1940-05-23 1940-05-23 Improvements in and relating to the manufacture of cyanoacrylic acid esters Expired GB541375A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB913140A GB541375A (en) 1940-05-23 1940-05-23 Improvements in and relating to the manufacture of cyanoacrylic acid esters

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB913140A GB541375A (en) 1940-05-23 1940-05-23 Improvements in and relating to the manufacture of cyanoacrylic acid esters

Publications (1)

Publication Number Publication Date
GB541375A true GB541375A (en) 1941-11-25

Family

ID=9865956

Family Applications (1)

Application Number Title Priority Date Filing Date
GB913140A Expired GB541375A (en) 1940-05-23 1940-05-23 Improvements in and relating to the manufacture of cyanoacrylic acid esters

Country Status (1)

Country Link
GB (1) GB541375A (en)

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