http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1844059-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5d4ada69388e0a1b68daaf536597c732
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-122
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-12
filingDate 2006-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f3712b88443eaa6733123a278892456e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae13735c5a738ad76df3e655067206ec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c718c8efe25482c28ffe9d08d4b13c3b
publicationDate 2007-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1844059-A1
titleOfInvention Method of making phenyl-containing chlorosilanes with aliphatic or cycloparaffinic hydrocarbon solvents
abstract Phenylmethyldichlorosilanes and diphenylmethylchlorosilanes are prepared by a Grignard process involving the step of contacting a phenyl Grignard reagent, an ether solvent, a trichlorosilane, and an aliphatic or cycloparaffinic hydrocarbon coupling solvent; in a mole ratio of the ether solvent to the phenyl Grignard reagent is 2 to 5, the mole ratio of the trichlorosilane to the phenyl Grignard reagent is 0.1 to 10, and the mole ratio of the aliphatic or cycloparaffinic hydrocarbon coupling solvent to the phenyl Grignard reagent is 3 to 7. Preferred reactants include phenylmagnesium chloride as the phenyl Grignard reagent; diethyl ether as solvent; n-heptane as the aliphatic hydrocarbon coupling solvent, or cyclohexane as the cycloparaffinic hydrocarbon coupling solvent; and methyltrichlorosilane.
priorityDate 2005-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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