http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1396826-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-90
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-90
filingDate 1973-04-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1975-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1396826-A
titleOfInvention Substituted 2-halo-4,5-dicyano-imidazoles and their preparations
abstract 1396826 Substituted 2-halo-4,5-dicyanoimidazoles E I DU PONT DE NEMOURS & CO 6 April 1973 [7 April 1972] 16610/73 Heading C2C The invention comprises compounds of formula where R contains up to 10 carbon atoms and is an alkyl, aryl, aralkyl, fluoro(oxaalkyl), haloalkyl or aryl(haloalkyl) group and X is F, Cl, Br or I, with the proviso that when X is I, R is only alkyl, aralkyl, fluoro(oxaalkyl) or haloalkyl, halo being F, Cl or Br. These compounds are prepared by reacting in the liquid phase at 50- 140‹ C. 2 - diazo - 4,5 - dicyano - 2H - imidazole with a compound of formula RX, where R and X are as defined above. When RX is chloro- or bromobenzene, a halonium compound of formula was detected in the reaction mixture; in the case of bromobenzene the halonium compound was found to rearrange to give 1-phenyl-2- bromo-4,5-dicyanoimidazole. With reactants RX containing C-H bonds, which may be written R<SP>1</SP>H, 4,5-dicyanoimidazoles substituted by R<SP>1</SP> in the 2 position are obtained as byproducts. In the examples, R is ethyl, various haloalkyl groups, phenyl, phenyl difluoromethyl and 2H-5-(trifluoromethyl)-perfluoro-3,6-dioxa- 2-nonyl.
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priorityDate 1972-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 26.