ES277959A1 - Procedure for the preparation of compounds of 1-methyl-1,2-di- [benzymidazoil- (2º)] - ethylene (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the preparation of compounds of 1-methyl-1,2-di- [benzymidazoil- (2º)] - ethylene (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES277959A1
ES277959A1 ES277959A ES277959A ES277959A1 ES 277959 A1 ES277959 A1 ES 277959A1 ES 277959 A ES277959 A ES 277959A ES 277959 A ES277959 A ES 277959A ES 277959 A1 ES277959 A1 ES 277959A1
Authority
ES
Spain
Prior art keywords
formula
translation
methyl
preparation
machine
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
ES277959A
Other languages
Spanish (es)
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.)
Novartis AG
BASF Schweiz AG
Original Assignee
Ciba Geigy AG
Ciba 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 Ciba Geigy AG, Ciba AG filed Critical Ciba Geigy AG
Publication of ES277959A1 publication Critical patent/ES277959A1/en
Expired legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/02Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/18Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds from polymers of unsaturated nitriles, e.g. polyacrylonitrile, polyvinylidene cyanide
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/28Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D01F6/38Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolymers obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising unsaturated nitriles as the major constituent

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Detergent Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Process for the preparation of 1-methyl-1,2-di- [benzimidazolyl- (2 ')] - ethylene compounds of the formula ** (See formula) ** in which A1 and A2 each represent a benzene radical, of which 2 neighboring cyclic carbon atoms belong at the same time to the imidazole ring, and X and Y each mean the complement of an imidazoic radical, characterized in that, at temperatures above 150º C and in the presence of phosphoric acids of the formula Hn+2PnO3n+1 where n means an integer, a dicarboxylic acid of the formula is reacted in the molecular ratio 1: 2 ** (See formula) ** wherein C3H4 means a radius to the single unsaturated hydrocarbon and the two carboxylic acid groups are linked to neighboring carbon atoms of the C3H4 radical, or a functional derivative of an acid of this nature, with at least one 1,2-diaminobenzene of which one amino group is primary, while the other amino group is at most secondary. (Machine-translation by Google Translate, not legally binding)
ES277959A 1961-06-05 1962-06-04 Procedure for the preparation of compounds of 1-methyl-1,2-di- [benzymidazoil- (2º)] - ethylene (Machine-translation by Google Translate, not legally binding) Expired ES277959A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH653161A CH415648A (en) 1961-06-05 1961-06-05 Process for the preparation of 1-methyl-1,2-di- (benzimidazolyl- (2 ')) -ethylenes and their application

Publications (1)

Publication Number Publication Date
ES277959A1 true ES277959A1 (en) 1963-01-01

Family

ID=4311059

Family Applications (1)

Application Number Title Priority Date Filing Date
ES277959A Expired ES277959A1 (en) 1961-06-05 1962-06-04 Procedure for the preparation of compounds of 1-methyl-1,2-di- [benzymidazoil- (2º)] - ethylene (Machine-translation by Google Translate, not legally binding)

Country Status (4)

Country Link
CH (1) CH415648A (en)
ES (1) ES277959A1 (en)
GB (1) GB941866A (en)
SE (1) SE309419B (en)

Also Published As

Publication number Publication date
SE309419B (en) 1969-03-24
CH415648A (en) 1966-06-30
GB941866A (en) 1963-11-13

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