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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-31
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-676
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-67
filingDate 1959-01-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5c8031583acc0a1ef437f958147fbfa
publicationDate 1962-01-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-886353-A
titleOfInvention Production of unsaturated ketones
abstract Unsaturated aliphatic ketones of the general formula R1.R2.C=CH.CH2.CH2.CO.R3 wherein R1 and R2 are alkyl or alkenyl groups or H atoms and R3 is an alkyl group, are prepared by contacting allyl aceto acetates of the general formula R1.R2.C(CH=CH2).O.CO.CH2.CO.R3 at an elevated temperature, e.g. 100 DEG C.-300 DEG C., with an aluminium enolate of the general formula Al(-O.C.R4=CH.CO.R5)3 wherein one of the groups R4 and R5 is an alkyl group and the other is an alkyl or alkoxy group. Specified aluminium enolates are the tri-acetylacetonate, obtainable by reacting aluminium sulphate with acetylacetone in aqueous NH3, and a tri-(alkylacetoacetate) obtainable by reacting an aluminium tri-alkoxide with, for example, methyl or ethyl aceto acetate. Examples describe the conversion of (1) 3-methyl but-1-enyl-3-aceto acetate to 2-methylhept-2-en-6-one, the catalyst being omitted in a comparative experiment; (2) 3-methyl-pent-1-enyl-3-aceto acetate to 3-methyl-oct-3-en-7-one; and (3) linalyl aceto acetate to geranyl acetone.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5874635-A
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priorityDate 1959-01-14-04:00^^<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: 35.