GB803567A - A process for the production of 1-ketocyclo-octyl-2-methylene compounds - Google Patents

A process for the production of 1-ketocyclo-octyl-2-methylene compounds

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Publication number
GB803567A
GB803567A GB28302/56A GB2830256A GB803567A GB 803567 A GB803567 A GB 803567A GB 28302/56 A GB28302/56 A GB 28302/56A GB 2830256 A GB2830256 A GB 2830256A GB 803567 A GB803567 A GB 803567A
Authority
GB
United Kingdom
Prior art keywords
octanone
cyclo
ketocyclo
octyl
methyl
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
GB28302/56A
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.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik 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 BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB803567A publication Critical patent/GB803567A/en
Expired legal-status Critical Current

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  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1-Ketocyclo octyl 4-methylene compounds of general formula <FORM:0803567/IV (b)/1> where X is nitrile carboxylic acid group or alkali metal salt thereof are prepared by reacting a tertiary 2-amino-methyl cyclo octanone (1) in the form of its salts or quaternization products thereof, with an alkali metal cyanide and if desired saponifying the resultant 2-(cyanomethyl)-cyclo-octanone (1). The tertiary 2-aminomethyl cyclo octanone (1) may be prepared by the Mannich reaction using cyclo-octanone with formaldehyde and secondary amines, e.g. dimethylamine, diethylamine, methylethylamine, pyrrolidine, piperidine or morpholine. The quaternization product or salt may then be obtained e.g. by reacting with hydrogen chloride, bromide or iodide or with methyl or ethyl bromide or iodide or with dimethyl sulphate or para toluene sulphonic acid ethyl ester. The reaction of these compounds with the alkali cyanides is preferably carried out in aqueous or aqueous alcoholic solution at 50 DEG to 80 DEG C. with excess sodium or potassium cyanide. The saponification of the nitrile is preferably effected by heating with aqueous caustic alkali solution and the 1-ketocyclo octyl 2-acetic acid is obtained from its salt by neutralization with hydrochloric or sulphuric acid. Examples are given for the preparation of 2-(cyanomethyl) cyclo octanone-(1) and 1-ketocyclo octyl-2-acetic acid from sodium cyanide and (1) 2-dimethylaminomethylcyclo octanone - (1) iodomethylate; (2) 2-trimethyl ammonium methyl-cyclo octanone-(1) methyl sulphate; (3) 2-dimethyl aminomethyl cyclo-octanone-(1) hydrochloride; (4) 2-piperidinomethylcyclo-octanone-(1) iodomethylate.
GB28302/56A 1955-09-28 1956-09-17 A process for the production of 1-ketocyclo-octyl-2-methylene compounds Expired GB803567A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE803567X 1955-09-28

Publications (1)

Publication Number Publication Date
GB803567A true GB803567A (en) 1958-10-29

Family

ID=6721931

Family Applications (1)

Application Number Title Priority Date Filing Date
GB28302/56A Expired GB803567A (en) 1955-09-28 1956-09-17 A process for the production of 1-ketocyclo-octyl-2-methylene compounds

Country Status (1)

Country Link
GB (1) GB803567A (en)

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