http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008007489-A

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filingDate 2006-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d19ca73dd4430ea506bff6d957e2f482
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f54c83196360dd9a103e7d0b7c4d2666
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publicationDate 2008-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2008007489-A
titleOfInvention Process for producing optically active 1- (fluoro, trifluoromethyl or trifluoromethoxy substituted phenyl) alkylamine N-monoalkyl derivatives
abstract The present invention provides an industrial process for producing optically active 1- (fluoro, trifluoromethyl or trifluoromethoxy substituted phenyl) alkylamine N-monoalkyl derivatives which are important intermediates for pharmaceuticals and agricultural chemicals. A fluoro, trifluoromethyl or trifluoromethoxy substituted phenyl alkyl ketone and an optically active primary amine are converted to an optically active imine by dehydration condensation, and then the imine is present in a hydrogen gas atmosphere in the presence of a transition metal catalyst. To an optically active secondary amine by asymmetric reduction, and further, reductive alkylation of the secondary amine and formaldehyde (including equivalents) or lower aldehyde in the presence of a transition metal catalyst in a hydrogen gas atmosphere By converting to an optically active tertiary amine and finally subjecting the tertiary amine to hydrogenolysis, the target optically active compound can be produced efficiently. [Selection figure] None
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID413282506
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547026
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426137234
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12085
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID10199821
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1512509
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426137237

Total number of triples: 309.