http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04120059-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D231-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
filingDate 1990-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_785382b23e58e5ff8613ffdf35a805a3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7b261ebeda34edbd2aceaa087da0132f
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publicationDate 1992-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04120059-A
titleOfInvention Production of substituted pyrazole-4-carboxylic acid
abstract PURPOSE: To obtain the subject compound known as a useful intermediate for an acid amide compound which is an active component of a fungicide for agricultural and horticultural use, at a low cost, by reacting a substituted pyrazole-4- carbaldehyde with sodium chlorite in the presence of hydrogen peroxide and a phase-transfer catalyst. n CONSTITUTION: The objective compound of formula II can be produced by reacting a compound of formula I (R 1 is methyl, ethyl or CF 3 ) with sodium chlorite in the presence of hydrogen peroxide and a phase-transfer catalyst (e.g. tetrabutylammonium bromide and crown ether) preferably in a solvent at pH2-6 and a temperature between 0°C and the boiling point of the solvent, preferably 10-70°C. Preferably, the amount of sodium chlorite and hydrogen peroxide is 1-2 equivalent each and that of the phase-transfer catalyst is 0.001-0.1 equivalent per 1 equivalent of the compound of formula I. n COPYRIGHT: (C)1992,JPO&Japio
priorityDate 1990-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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