http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4391984-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_424db9d56b06a23aed410fcf5df652f3
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-283
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-2632
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-26
filingDate 1981-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1983-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfae59e959d199a8d35045973e8bd022
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_597b4f551125092134ad384f1d099624
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_88fcaf1b13d32bc02dfc97840e6ad735
publicationDate 1983-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4391984-A
titleOfInvention Alkynyl halide compounds and alkenyl acetate compounds therefrom
abstract The invention provides a novel method for the synthetic preparation of an ω-haloalkyne compound of the general formula R--C.tbd.C--CH 2 ) n X, in which X is a halogen atom, R is a monovalent hydrocarbon group and n is 4, 5 or 6, by the coupling reaction of a Grignard reagent RMgX' and an ω-halo-1-bromoalkyne compound of the formula X--CH 2 ) n C.tbd.C-Br. The ω-haloalkyne compound obtained in the above can be readily converted to the corresponding alkenyl acetate of the formula R--CH═CH--CH 2 ) n OCOCH 3 by first acetylating and then partially hydrogenating in the presence of a Lindlar catalyst. In particular, 7, 11-hexadecadienyl acetate, which is a sexual pheromone compound of a noxious insect, is obtained in the same route of synthesis starting with the Grignard reagent of a 1-halo-3-octene and 1, 8-dibromo-1-octyne.
priorityDate 1980-05-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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