http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014189487-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43000a5cfa837b51a2a690856b95ada2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9df90d7822cc480ce12c480f4089e229
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C50-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C46-06
filingDate 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93529eabd38abe110ac2a7f409e5320d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f53bdbb364e1cad5e88a090dcdbb3e8b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5dd23c560f0986f05598bc79f6fa166
publicationDate 2014-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2014189487-A
titleOfInvention Method for producing 1,4-benzoquinones
abstract The present invention provides an efficient method for producing a 1,4-benzoquinone compound that is extremely useful as a synthetic intermediate for pharmaceuticals, agricultural chemicals, and the like. A phenol represented by the formula (A) is reacted in an alcohol solvent, preferably an ethanol solvent, in the presence of a copper halide and a hydroxylamine compound, at a reaction temperature of 0 ° C to 90 ° C, preferably 20 ° C. Corresponding 1,4-benzoquinones are produced by oxidation with hydrogen peroxide at -30 ° C. [Wherein, X represents hydrogen or a hydroxyl group, and R 1 , R 2 , R 3 , and R 4 represent hydrogen and an alkyl group, an alkoxy group, an alkylsulfonyl group, an aryl group, an aryloxy group that may have a substituent. And a group independently selected from the group consisting of a group, an arylsulfonyl group, an aralkyl group, a hydroxyl group and a halogen. ] [Selection figure] None
priorityDate 2013-03-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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