GB1007413A - Process for the preparation of n-substituted imido chlorides, or hydrochloric salts thereof, from ketoximes - Google Patents

Process for the preparation of n-substituted imido chlorides, or hydrochloric salts thereof, from ketoximes

Info

Publication number
GB1007413A
GB1007413A GB2368164A GB2368164A GB1007413A GB 1007413 A GB1007413 A GB 1007413A GB 2368164 A GB2368164 A GB 2368164A GB 2368164 A GB2368164 A GB 2368164A GB 1007413 A GB1007413 A GB 1007413A
Authority
GB
United Kingdom
Prior art keywords
gives
hydrochloride
ketoximes
chlorides
preparation
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
GB2368164A
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.)
Stamicarbon BV
Original Assignee
Stamicarbon BV
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 Stamicarbon BV filed Critical Stamicarbon BV
Publication of GB1007413A publication Critical patent/GB1007413A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides

Landscapes

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

Abstract

An N-substituted imidochloride or mixture thereof is prepared by reacting a ketoxime or a hydrohalide thereof with phosgene in the absence of water, at a temperature which from or after the commencement of the reaction exceeds 20 DEG C., in such a way that at all or substantially all times while the reaction temperature is above 20 DEG C., not more than two mols. of phosgene are available per mol. of ketoxime. Preferably a polar solvent is used, e.g. nitromethane, nitrocyclohexane, chlorobenzene, chloroform, acetonitrile or benzonitrile. In examples: (1) benzophenone oxime gives N-phenylbenzimidochloride; (2) acetophenone oxime gives N-phenylacetimidochloride; (3) diethylketoxime gives N-ethylpropionimidochloride hydrochloride; (4) cyclohexenone oxime gives 2-chloroazacyloheptene-1,2 hydrochloride, which with aniline yields 2-phenylaminoazacyclo-1,2-heptene; (5) cycloheptanone oxime gives 2-chloroazacyclo-1,2-octene hydrochloride which with aniline yields the anilido compound. Specification 999,880 is referred to
GB2368164A 1963-06-11 1964-06-08 Process for the preparation of n-substituted imido chlorides, or hydrochloric salts thereof, from ketoximes Expired GB1007413A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL293908 1963-06-11

Publications (1)

Publication Number Publication Date
GB1007413A true GB1007413A (en) 1965-10-13

Family

ID=19754769

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2368164A Expired GB1007413A (en) 1963-06-11 1964-06-08 Process for the preparation of n-substituted imido chlorides, or hydrochloric salts thereof, from ketoximes

Country Status (5)

Country Link
BE (1) BE649064A (en)
CH (1) CH454831A (en)
DE (1) DE1230786B (en)
GB (1) GB1007413A (en)
NL (1) NL293908A (en)

Also Published As

Publication number Publication date
NL293908A (en)
CH454831A (en) 1968-04-30
DE1230786B (en) 1966-12-22
BE649064A (en) 1964-12-10

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