GB788436A - Improvements in the production of cycloaliphatic ketoximes and their hydrochlorides - Google Patents

Improvements in the production of cycloaliphatic ketoximes and their hydrochlorides

Info

Publication number
GB788436A
GB788436A GB23098/56A GB2309856A GB788436A GB 788436 A GB788436 A GB 788436A GB 23098/56 A GB23098/56 A GB 23098/56A GB 2309856 A GB2309856 A GB 2309856A GB 788436 A GB788436 A GB 788436A
Authority
GB
United Kingdom
Prior art keywords
hydrochlorides
chloride
hydrogen chloride
hydrocarbon
nitric oxide
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
GB23098/56A
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 GB788436A publication Critical patent/GB788436A/en
Expired legal-status Critical Current

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

Abstract

Cycloaliphatic ketoximes and their hydrochlorides are prepared by the reaction of cycloaliphatic hydrocarbons with nitrosyl chloride in the presence of added hydrogen chloride and/or nitric oxide while irradiating with light to form the hydrochlorides and, if required, treating the hydrochlorides with an inorganic base to form the free ketoximes. Suitable cycloaliphatic hydrocarbons are cyclopentane, cyclohexane, cycloheptane and cyclo-octane and their alkyl substituted derivatives. The process may be carried out at a temperature varying from - 50 DEG C. to 40 DEG C. The hydrogen chloride may be dissolved in the hydrocarbon with nitrosyl chloride, or a mixture of nitrosyl chloride and hydrogen chloride may be pumped through the hydrocarbon. The nitric oxide is preferably pumped with nitrosyl chloride through the hydrocarbon, and hydrogen chloride may be mixed with the nitric oxide. In the examples cyclopentanone oxime, cyclohexanone oxime, cyclo-octanone oxime and isomeric ketodecahydronaphthalene oximes and their hydrochlorides are prepared.
GB23098/56A 1955-08-05 1956-07-26 Improvements in the production of cycloaliphatic ketoximes and their hydrochlorides Expired GB788436A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE788436X 1955-08-05

Publications (1)

Publication Number Publication Date
GB788436A true GB788436A (en) 1958-01-02

Family

ID=6699466

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23098/56A Expired GB788436A (en) 1955-08-05 1956-07-26 Improvements in the production of cycloaliphatic ketoximes and their hydrochlorides

Country Status (1)

Country Link
GB (1) GB788436A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1240074B (en) * 1963-07-03 1967-05-11 Toyo Rayon Co Ltd Process for the preparation of cycloalkanone oximes by photonitrosation of C -C cycloalkanes

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1240074B (en) * 1963-07-03 1967-05-11 Toyo Rayon Co Ltd Process for the preparation of cycloalkanone oximes by photonitrosation of C -C cycloalkanes

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