http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9365477-B2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_33dafb5bbc2ec47ebcb7becbbe60f704
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-51
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-00
filingDate 2014-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2016-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_36a3a95cf00105974e7ecb9b4941079b
publicationDate 2016-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9365477-B2
titleOfInvention Method for producing lavandulal
abstract Provided is a method of producing lavandulal at a high yield by controlling formation of its isomer of lavandulal as a by-product. n In a method of producing lavandulal by making an acetal compound represented by the following formula (I) react with 3-methyl-1-butene-3-ol in the presence of an acid catalyst, the method includes: adding, to a liquid mixture comprising an acid catalyst, an acetal compound represented by the following formula (I), and 3-methyl-1-butene-3-ol in at least a portion of an amount to be used (3-methyl-1-butene-3-ol (a)), 3-methyl-1-butene-3-ol in the other portion of the amount to be used (3-methyl-1-butene-3-ol (b)); and maintaining the liquid mixture at a temperature of 110° C. or higher: n nin which Each R in the formula (I) represents an alkyl group.
priorityDate 2013-03-19-04:00^^<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: 49.