http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000063323-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 1999-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fef4354898c03c26f509234196cf1722
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8d9620a893905c1fd8ee2cce802576a5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2cc9a2ef26f100e05fce581970ec661e
publicationDate 2000-02-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000063323-A
titleOfInvention Synthesis of tert-butyl o- (p-tolyl) benzoate by reaction of o- (p-tolyl) benzoic acid and isobutylene under acid catalysis
abstract (57) [Problem] To provide a method for easily and inexpensively obtaining tert-butyl o- (p-tolyl) benzoate with high purity and high yield. SOLUTION: The present invention relates to a tert-butyl o- A process for producing (p-tolyl) benzoate, comprising: Fluorosulfonic acid catalytic activity amount, trifluoromethanesulfonic acid, straight-chain or branched perfluoro (C 2 ~ The presence of C 8) alkyl sulfonic acid, linear or branched partially fluorinated (C 2 ~C 8) alkylsulfonic acids, partially fluorinated (C 5 ~C 6) cycloalkyl sulfonic acid or mixtures of these acids And a method comprising reacting o- (p-tolyl) benzoic acid with isobutylene.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010275298-A
priorityDate 1998-08-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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