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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D271-113
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D271-10
filingDate 2012-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7995eb9c581a7bf1e68f86ad72559705
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b16e02329c4f66c9de623cef651b807
publicationDate 2014-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2014101322-A
titleOfInvention Method for producing oxadiazolinone compound
abstract An object of the present invention is to provide a novel method capable of producing an oxadiazolinone compound (VI) from a diazonium salt in a good yield. A process for producing an oxadiazolinone compound (VI) comprising a diazonium salt (I), at least one selected from the group consisting of sulfites and hydrogen sulfites, and water at a pH of 5.5 to 7 After mixing at 45 to 100 ° C. in the range of 0.5, the resulting mixture is heat-treated at 45 to 100 ° C. and then subjected to contact treatment with acid (A), obtained in step (A). The step (B) of reacting the phenylhydrazine compound (II) with the halogenated alkyl carbonate (III) or dialkyl dicarbonate (IV), and the phenylhydrazine-β-carboxylate compound obtained in the step (B) ( V) and phosgene are reacted, and then the step (C) is brought into contact with a basic compound. [Selection figure] None
priorityDate 2012-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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