http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2000336074-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C315-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C315-04
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filingDate 2000-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44c755f7850ebea9f4ef9bccd432bcbd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aa5c47a1ca3f7623e08909dad89b6179
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43441dc1799535047aa77f1c4c9f77dc
publicationDate 2000-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000336074-A
titleOfInvention Method for producing [2- (arylsulfonyl) ethenyl] benzene derivative
abstract [PROBLEMS] To provide a safe and efficient method for producing [2- (arylsulfonyl) ethenyl] benzene derivatives. The corresponding general formula 1 Reaction of 2- (arylsulfonyl) ethanols with an acid anhydride in the presence of a base, Aromatic chlorine, bromine or iodide, the general formula 3 to act in the presence of P d catalyst and a base (R 1 to R 4 are the same or different and are hydrogen, fluorine, chlorine, lower alkyl, lower alkoxy, nitro, cyano, Represents an amino, lower alkylamino, di (lower alkyl) amino, acyl or alkoxycarbonyl group. Here, when R 3 and R 4 are adjacent to each other, they may form a ring together. [2- (arylsulfonyl) ethenyl] A method for producing a benzene derivative.
priorityDate 1999-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421348141
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID300030
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID416171943
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11457
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID140387

Total number of triples: 309.