http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2012188419-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C41-09
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
filingDate 2012-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_082c712e07b8b4b8854e8fad9edf0ff3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21c19167680d99b97fd8ffc116353101
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publicationDate 2012-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2012188419-A
titleOfInvention Method for producing asymmetric allyl ether compound
abstract The present invention provides a production method that can be applied to a wide range of alcohols without using halogen, strong acid, or the like, and that can obtain an asymmetric allyl ether compound with high selectivity. An allyl alcohol represented by R 1 CH═CH—CH 2 OH is reacted with an alcohol represented by R 2 OH in the presence of a palladium compound and a specific triaryl phosphite. (Wherein, R 1 represents a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, an alkynyl group or alkadienyl group having 4 to 10 carbon atoms of 2 to 10 carbon atoms, R 2 Represents an alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkynyl group having 2 to 10 carbon atoms, each of which may have one or more hydroxyl groups at arbitrary positions. The manufacturing method of the asymmetrical allyl ether compound shown by these. [Selection figure] None
priorityDate 2011-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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