http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H01226856-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09K19-34
filingDate 1988-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf1279d98782c00b7ed8767a8017b2f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a48cb8be90afcd3b9f41ff9c47b2ea2
publicationDate 1989-09-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H01226856-A
titleOfInvention Optically active ethers and production thereof
abstract NEW MATERIAL:A compound shown by I [R is 1W20C alkyl or alkoxyalkyl; R' is 1W15C alkyl or group shown by formula II (A is H, lower alkyl, lower alkoxyl or halogen); l is 1 or 2; * is asymmetric carbon]. n EXAMPLE: Methyl (+)-4-(1-propoxyethyl)benzoate. n USE: An intermediate for drugs and agricultural chemicals. Useful as an intermediate especially for organic electronic materials, above all for a novel liquid crystalline substance. n PREPARATION: An optically active alcohol shown by formula III (R' is 1W15C alkyl or group shown by formula II) is reacted with an alkylating agent shown by the formula R-X ([X is halogen or -OSO 2 R''' (R''' is lower alkyl or phenyl which may be replaced)] in the presence of a base (e.g. NaOH) in a solvent such as THF at -50W120°C to give a compound shown by formula I. n COPYRIGHT: (C)1989,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2526629-B2
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priorityDate 1988-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 29.