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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-92
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 1995-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1367ecf333962c2427c63b20bcc9dc6d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a6556449fb4c51ce284dd2cca2ee192
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_559aeef129116eba81ad67a21ea9df50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_70918b1609a90792db1a242776c5720b
publicationDate 1996-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08231476-A
titleOfInvention Method for producing alkoxy-substituted triphenylamines
abstract (57) Abstract: De-alkoxylation of raw materials and intermediates is suppressed, and desired alkoxy group-substituted triphenylamines are obtained in good yield. SOLUTION: In the presence of a hydrogen transfer catalyst and a catalytic amount of alkoxy group-substituted cyclohexanones corresponding to the alkoxy group-substituted phenols used in the reaction, the above-mentioned alkoxy group-substituted phenols are used as a hydrogen acceptor, and in-system An alkoxy group-substituted triphenyl, characterized in that a surface-supported catalyst is used as a hydrogen transfer catalyst when reacting the cyclohexanones with diphenylamines while generating alkoxy group-substituted cyclohexanones from the alkoxy group-substituted phenols. Method for producing amines.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2020000963-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019098283-A
priorityDate 1994-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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