http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01226852-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C65-21
filingDate 1988-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a48cb8be90afcd3b9f41ff9c47b2ea2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf1279d98782c00b7ed8767a8017b2f8
publicationDate 1989-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01226852-A
titleOfInvention Production of optically active benzene derivative
abstract NEW MATERIAL:An optically active benzene derivative shown by formula I (R is 1W20C alkyl or alkoxyalkyl; A is H, lower alkyl, lower alkoxy or halogen; n is 1 or 2; * is asymmetric carbon). n EXAMPLE: (+)-4-(1-S-2'-Methylbutoxyethyl)benzoic acid. n USE: Useful as an intermediate for agricultural chemicals, drugs, etc. and also suitable as an intermediate for liquid crystal compounds. n PREPARATION: An optical active ether derivative shown by formula II (A is H, lower alkyl, lower alkoxy or halogen) is debenzylated to give a compound shown by formula I. The debenzylation reaction is usually carried out by catalytically hydrogenating with hydrogen in the presence of a hydrogenating catalyst or hydrolysis. The amount of the catalyst used is preferably 0.05W0.3pt.wt. based on 1pt.wt. compound shown by formula II. The reaction is carried out preferably at 10°CW60°C. n COPYRIGHT: (C)1989,JPO&Japio
priorityDate 1988-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 22.