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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-10
filingDate 1990-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1aa786e337e3073ccacdb9e726e70696
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2504be40f8489c08c4b2e50585fc0ec1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a7b74ba11c4d23b56bff843027b7475
publicationDate 1992-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04261143-A
titleOfInvention Production of 1-n,n-diphenylaminopyrene derivative
abstract PURPOSE: To readily obtain a 1-N,N-diphenylaminopyrene derivative useful as an electrophotographic organic photoconductive material by reacting a 1- halogenopyrene used as a raw material with a diphenylamine derivative. n CONSTITUTION: A 1-halogenopyrene (e.g. 1-iodopyrene) expressed by formula I (X is halogen) is reacted with a diphenylamine derivative (e.g. 4,4'- dimethyldiphenylamine) expressed by formula II (R 1 and R 2 are H, halogen, cyano-substituted or unsubstituted alkyl, alkoxy or phenyl), preferably in the presence of copper powder, copper oxide or a copper halide in or without a solvent in an atmosphere of nitrogen by adding an alkaline salt in an amount sufficient to neutralize hydrogen halides formed as a by-product in the condensing reaction. Thereby, a 1-N,N-diphenylaminopyrene derivative [e.g. 1-N,N-bis (4-methylphenyl)aminopyrene] expressed by formula III is obtained. The resultant compound is useful also as a charge transport substance in function separating type photosensitive units. n COPYRIGHT: (C)1992,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4536365-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2004217638-A
priorityDate 1990-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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