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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-21
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B49-00
filingDate 2007-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2009-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_195b6b5ea6782cf1014cfc4a8eca1cb1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1ef1bfc5ccb7ba25997f2b27e602b8d4
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publicationDate 2009-02-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-100462348-C
titleOfInvention Synthetic method for 2,6-dimethy-5-heptenal
abstract The invention discloses a synthesizing method of 2, 6-dimethyl-5-heptene aldehyde, which comprises the following steps: 1) dissolving 6-methyl-5-heptene-2-ketone and aluminium isopropoxide with molar rate at 1:0.35-1 into benzene or toluene solution; reducing under 60-120 deg.c; hydrolyzing into 6-methyl-5-heptene-2-alcohol; 2) halogenating 6-methyl-5-heptene-2-alcohol and halogenating agent with molar rate at 1:0.35-2 under -10-80 deg.c to produce 2-chlorine-6-methyl-5-heptene or 2-bromine-6-methyl-t-heptene; 3) reacting 2-chlorine-6-methyl-5-heptene or 2-bromine-6-methyl-t-heptene and magnesium to produce Grignard reagent; allocating the composition and formic ether with molar rate at 0.5-1:1 under -10-30 deg.c to do Grignard additional reaction; hydrolyzing; decompressing; distilling; obtaining the product.
priorityDate 2007-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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