http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0491256-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8b9b07baa39efdd68eb1506a375245f8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B11-18
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B11-00
filingDate 1991-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3422eb0be93f6fb2ab3d52b033aa6d0f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_564709a2aa01982a4dfb29fb9bc30f24
publicationDate 1992-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0491256-A1
titleOfInvention Process for the preparation of triphenylmethane dyes
abstract A process for the preparation of triphenylmethane dye of the formula:n n wherein An ⊖ denotes the equivalent of an anion, nR₁ and R₂ each denote hydrogen, C₁-C₄ alkyl, benzyl or hydroxysulfonylbenzyl, nR₃ and R₄ each denote hydrogen, C₁-C₄ alkyl or hydroxysulfonyl, nR₅ denotes phenyl, hydroxysulfonyl, C₁-C₄ dialkylaminophenyl, C₁-C₄ alkylphenyl, C₁-C₄ alkyl-C₁-C₄-dialkylaminophenyl, halogenophenyl, naphthyl, hydroxysulfonylnaphthyl, dihydroxysulfonylnaphthyl, or C₁-C₄ alkyldihydroxysulfonyl comprisingn I. oxidation of the leuco compound of the corresponding triphenylmethane dye with manganese dioxide in the presence of an aqueous acid at a temperature of about 20°C to about 100°C, II. adding optionally a salt of phosphoric acid and adding a base selected from the group consisting of ammonia, amines, aminoalcohols, metal hydroxides of Groups IA, IIA, IIIA and mixtures thereof in an amount sufficient to neutralize the aqueous solution, III. filtration from the precipitate and IV. isolation of said triphenylmethane dye.
priorityDate 1990-12-18-04:00^^<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: 56.