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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-62
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-56
filingDate 1977-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_118d96191f5459b618bea88a8bd7f329
publicationDate 1982-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-631174-A5
titleOfInvention Process for the preparation of 2,5-bis-(benzoxazolyl)-thiophene compounds
abstract A process for the preparation of 2,5-bis-(benzoxazolyl)-thiophene compounds of the formula <IMAGE> wherein R1 denotes hydrogen, halogen, optionally substituted alkyl, alkenyl, cycloalkyl, alkoxy, optionally substituted phenyl or phenoxy, carboxyl or its functional derivatives including cyano, sulpho and its functional derivatives or alkylsulphonyl, R2 denotes hydrogen, alkyl, halogen or alkoxy, R3 denotes hydrogen, chlorine or alkyl and R4 and R5 each denote hydrogen or alkyl or conjointly denote the trimethylene or tetramethylene radical, in which process a sulphide of formula <IMAGE> is reacted with an alpha , beta -dicarbonyl compound of formula R4-CO-CO-R5, or with a functional derivative of such a compound, preferably in an inert solvent, in the presence of an acid or a base, especially in the presence of an alkali metal alcoholate or alkali metal hydroxide. The compounds produced are valuable optical brighteners for organic materials.
priorityDate 1977-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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