http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08268976-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-52 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-52 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J23-42 |
filingDate | 1995-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cf047638fe93365edfef7e3160954065 |
publicationDate | 1996-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H08268976-A |
titleOfInvention | Method for producing 1-chloro-substituted phenylalkylamines |
abstract | (57) [Summary] (Correction) [Constitution] General formula [I] A method for producing 1-chloro-substituted phenylalkylamines of the general formula II, which comprises catalytically hydrogenating chloro-substituted phenylalkylketone oxime acetates of 1 above in the presence of an organic carboxylic acid solvent and a platinum catalyst. (R 1 represents a lower alkyl group, and R 2 represents a hydrogen atom or a chlorine atom.) [Effect] Even under low pressure, 1-chloro is efficiently produced in a high yield with almost no alcohol by-product. Substituted phenylalkylamines II can be prepared. |
priorityDate | 1995-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 105.