GB877407A - Process for the production of ª--cyan-ª--alkyl-ª--phenyl acrylic esters - Google Patents

Process for the production of ª--cyan-ª--alkyl-ª--phenyl acrylic esters

Info

Publication number
GB877407A
GB877407A GB23341/60A GB2334160A GB877407A GB 877407 A GB877407 A GB 877407A GB 23341/60 A GB23341/60 A GB 23341/60A GB 2334160 A GB2334160 A GB 2334160A GB 877407 A GB877407 A GB 877407A
Authority
GB
United Kingdom
Prior art keywords
alkyl
acid
ketimine
phenyl
substituted
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
GB23341/60A
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.)
Bayer AG
Original Assignee
Bayer AG
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 Bayer AG filed Critical Bayer AG
Publication of GB877407A publication Critical patent/GB877407A/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

a -cyano-b -alkyl-b -phenyl acrylic acid esters are prepared by reacting an N-alkyl substituted alkyl phenyl ketimine with a cyanoacetic acid ester in the presence of at least the stoichiometric amount of acid. The ketimine may be first prepared by reacting an alkyl phenyl ketone, in which the ring may be substituted e.g. by alkyl or alkoxy groups, with a primary alkylamine and the so-obtained ketimine reacted with the cyano ester optionally in the presence of an organic solvent. The acid may be organic or inorganic and acetic acid is preferably used. In examples ketimines obtained from cyclohexylamine and acetophenone, p-methoxyacetophenone and propiophenone are reacted with methyl and nonyl cyanoacetates to give the corresponding substituted acrylates.
GB23341/60A 1959-07-04 1960-07-04 Process for the production of ª--cyan-ª--alkyl-ª--phenyl acrylic esters Expired GB877407A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE877407X 1959-07-04

Publications (1)

Publication Number Publication Date
GB877407A true GB877407A (en) 1961-09-13

Family

ID=6818086

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23341/60A Expired GB877407A (en) 1959-07-04 1960-07-04 Process for the production of ª--cyan-ª--alkyl-ª--phenyl acrylic esters

Country Status (1)

Country Link
GB (1) GB877407A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3253979A (en) * 1963-06-20 1966-05-31 Olin Mathieson Light stabilized chlorine compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3253979A (en) * 1963-06-20 1966-05-31 Olin Mathieson Light stabilized chlorine compositions

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