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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-70
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0237
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0235
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-006
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-08
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D451-14
filingDate 2005-06-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2008-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-WO2006001387-A1
titleOfInvention Alcohol oxidation catalyst and synthesis method thereof
abstract The present invention proposes an organic oxidation catalyst for alcohols which is excellent in environmental harmony and enables more efficient oxidation, and a synthesis method thereof. 1-Alkyl-2-azaadamantane-N-oxyl synthesized with a nitroxyl group on the adamantane skeleton, synthesized from a bicyclo isomer obtained by Grob-type ring cleavage reaction of 1,3-adamantanediol, as an alcohol As an oxidation catalyst. By having a nitroxyl group on the adamantane skeleton, hydrogen at the α-position is stabilized by the Bredt rule, and the stability of the oxoammonium group generated by oxidation of this is guaranteed, and steric hindrance compared to TEMPO, which is a conventional oxidation catalyst Decreases and a wide reaction field can be secured. For this reason, the secondary alcohol having a sterically complicated structure, which is difficult to oxidize with TEMPO, can be oxidized with high efficiency, as well as the oxidation of the primary alcohol.
priorityDate 2004-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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