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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_38b04dac5e5700071e574cb587f8e099
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-50
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F9-30
filingDate 1993-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c1f622595ecba0df9323e0e3528d9b03
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a57dd20b22751016d3ff9937767f142e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_46eb65a7d0e9aaa40b5e0c9600362746
publicationDate 1995-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07188264-A
titleOfInvention Method for producing phosphinylcarboxylic acid
abstract (57) [Summary] (Modified) [Structure] An organic dichlorophosphine and (meth) acrylic acid are reacted to form phosphonylcarbonyl chloride, which is then hydrolyzed to give a phosphinylcarboxylic acid of the general formula 3. In the production of, the hydrolysis is carried out in the presence of an oxidizing agent, or an oxidation treatment is carried out after the hydrolysis. (R 1 is an alkyl group, a substituted or unsubstituted aryl group, R 2 represents a hydrogen atom or a methyl group. [Effect] A highly pure, non-coloring phosphinylcarboxylic acid can be industrially advantageously produced. This compound is an extremely useful raw material for industrial intermediates of organic phosphorus compounds, reactive flame retardants, and the like.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100632988-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007238940-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-19990070137-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007238616-A
priorityDate 1993-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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