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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B47-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22
filingDate 1996-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7a60e92b20290456e94e6db5a1d5b163
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6bd40d4154a3e5e39276ce0c925f618f
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publicationDate 1998-04-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1088017-A
titleOfInvention Method for producing naphthalocyanine compound
abstract (57) [Summary] [PROBLEMS] To use an economical raw material and a reaction solvent, Provided is a method for producing a naphthalocyanine compound with high yield and high purity. SOLUTION: In a method for producing a naphthalosinin compound represented by the following general formula (I), 2,3- Using a naphthalenedicarboxylic acid compound, a 2,3-naphthalenedicarboxylic anhydride compound, a 2,3-naphthalenedicarboxylic acid imide compound, a 2,3-naphthalenedicarboxylic diamide compound or a 2,3-naphthalenedinitrile compound, Alternatively, a metal derivative, urea, and a catalyst are reacted using sulfolane as a reaction solvent. Embedded image (Wherein, R independently represents a halogen atom, an alkyl group, an aryl group, an alkoxy group, an alkylthio group, an arylthio group, a nitro group, or a dialkylamino group, M represents two hydrogen atoms, a divalent metal, Represents a divalent or tetravalent metal derivative, and n represents an integer of 0 to 6.)
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022130925-A1
priorityDate 1996-09-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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