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GB497485A - Manufacture of substituted acid amides - Google Patents

Manufacture of substituted acid amides

Info

Publication number
GB497485A
GB497485A GB1691537A GB1691537A GB497485A GB 497485 A GB497485 A GB 497485A GB 1691537 A GB1691537 A GB 1691537A GB 1691537 A GB1691537 A GB 1691537A GB 497485 A GB497485 A GB 497485A
Authority
GB
United Kingdom
Prior art keywords
yield
chloracetamide
chloride
pyridine
bromopropionamide
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
GB1691537A
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 GB1691537A priority Critical patent/GB497485A/en
Publication of GB497485A publication Critical patent/GB497485A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

Amides containing a tertiary amino or a quaternary ammonium group are obtained by the action of a heterocyclic secondary amine, or an aliphatic or heterocyclic tertiary amine which is unsubstituted or substituted only by hydrocarbon radicles, on an amide of either of the formulae XRCONHR1 or XR11(CONHR1)2, where X is chlorine or bromine, R is an alkylene group of not more than seven carbon atoms, R1 is hydrogen or hydroxymethyl, and R11 is a trivalent saturated aliphatic hydrocarbon radicle. Specified amides which may be treated are chloracetamide, chloromalonamide, b -bromopropionamide and N-hydroxymethyl-chloracetamide. Specified amines which may be used are piperidine, morpholine, triethylamine, trimethylamine, N-methylpiperidine, N-cetylpiperidine, N-benzylpiperidine, pyridine, a -picoline and quinoline. Examples are given in which (1) piperidine and chloracetamide yield piperidylacetamide, (2) pyridine and chloromalonamide yield di(carbamyl)methylpyridinium chloride, (3) pyridine and N-hydroxymethylchloracetamide yield (N-hydroxymethylcarbamyl)methylpyridinium chloride, (4) pyridine and b -bromopropionamide yield b -carbamylethylpyridinium bromide, (5) pyridine and chloracetamide yield carbamyl-methylpyridinium chloride, (6) benzylpiperidine and chloracetamide yield carbamylmethylbenzylpiperidinium chloride, (7) triethylamine and chloracetamide yield carbamylmethyltriethylammonium chloride. The products are useful in the treatment of textiles. b -Bromopropionamide is obtainable from ammonia and b -bromopropionyl chloride, which may be prepared from b -bromopropionic acid and thionyl chloride.
GB1691537A 1937-06-17 1937-06-17 Manufacture of substituted acid amides Expired GB497485A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1691537A GB497485A (en) 1937-06-17 1937-06-17 Manufacture of substituted acid amides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1691537A GB497485A (en) 1937-06-17 1937-06-17 Manufacture of substituted acid amides

Publications (1)

Publication Number Publication Date
GB497485A true GB497485A (en) 1938-12-19

Family

ID=10085965

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1691537A Expired GB497485A (en) 1937-06-17 1937-06-17 Manufacture of substituted acid amides

Country Status (1)

Country Link
GB (1) GB497485A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2973362A (en) * 1959-07-24 1961-02-28 Schorsch Gerald Method of preparing monosubstituted piperazines
US3354167A (en) * 1964-06-23 1967-11-21 Delmar Chem Pyrazolone derivatives and process for their preparation
US4424284A (en) 1980-10-28 1984-01-03 Ciga-Geigy Corporation Cationic adsorption agent

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2973362A (en) * 1959-07-24 1961-02-28 Schorsch Gerald Method of preparing monosubstituted piperazines
US3354167A (en) * 1964-06-23 1967-11-21 Delmar Chem Pyrazolone derivatives and process for their preparation
US4424284A (en) 1980-10-28 1984-01-03 Ciga-Geigy Corporation Cationic adsorption agent

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