http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H1160545-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C215-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-44
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-02
filingDate 1997-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f0c1e917bd976e4bceef5d761b7aa23
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10a977136f55db2cd6daad0aab417cb5
publicationDate 1999-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1160545-A
titleOfInvention Method for producing 2,2-bis (3-amino-4-hydroxyphenyl) propane
abstract PROBLEM TO BE SOLVED: To provide a high yield and high purity by a series of steps of producing a dinitro form of bisphenol A without leaving a nitrate group, and then reducing the dinitro form without leaving a metal of a catalyst. Provided is a method for producing 2,2-bis (3-amino-4-hydroxyphenyl) propane, which is the target substance. SOLUTION: First, an acetic acid solution of bisphenol A is added with 21. The required amount of concentrated nitric acid is added dropwise at a temperature of ~ 100 ° C, and then the remaining concentrated nitric acid is added dropwise at a temperature of 0 to 20 ° C to obtain a corresponding dinitro compound. Reduction using a palladium catalyst and hydrazine, and after the completion of the reduction reaction, removing all solvents including hydrazine to obtain a target product, 2,2-bis (3-amino-4-hydroxyphenyl) propane Take the process.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2009221117-A
priorityDate 1997-08-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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