http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05331106-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_630b360599ea5cf4b5bcbc0c6c0a3e2d |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-327 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-612 |
filingDate | 1992-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_753c55cd16e1303bfc69cadb7db63666 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4a5f0073a5dbcdc7c739505da4c7025 |
publicationDate | 1993-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H05331106-A |
titleOfInvention | Method for producing phenylacetic acid derivative |
abstract | (57) [Summary] [Structure] The arylaldehyde derivative represented by the following general formula (I) is reacted with hydrocyanic acid to obtain a mandelonitrile derivative represented by the following general formula (II), and the obtained mandelonitrile is obtained. The derivative is hydrolyzed to obtain an α-hydroxycarboxylic acid derivative represented by the following general formula (III), and further, A process for producing a phenylacetic acid derivative represented by the following general formula (IV), characterized in that the α-hydroxycarboxylic acid derivative is hydrolyzed as it is or after acetylating the α-position hydroxyl group. [Effect] The phenylacetic acid derivative can be obtained easily and in high yield. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103450009-A |
priorityDate | 1992-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 56.