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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-12
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J27-13
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
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filingDate 2000-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dc47f185a777eaf2d4e9932339c3de9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_44786a7c9ebe69269269df6aff2fb9ad
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publicationDate 2000-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2000351785-A
titleOfInvention Silicon compound containing silamethylene bond and method for producing the same
abstract PROBLEM TO BE SOLVED: To provide a novel organosilicon compound useful as an intermediate for producing silicon carbide and a method for producing the same. SOLUTION: Bis (dichlorosilyl) methanes, for example, bis (dichlorosilyl) methane are prepared by adding an unsaturated organic silane such as dichloromethylvinylsilane and an organic solvent such as benzene in the presence or absence of an organic solvent. 1 to 10 The molar ratio of the unsaturated organic silane to bis (dichlorosilyl) methane, bis (dichlorosilyl) 1 × 10 -5 to 0.05 moles of platinum group metal catalyst as a metal amount per 1 mol of methane, for example, H 2 PtCl The reaction is carried out at a temperature of 10 to 150 ° C. for 0.5 to 20 hours in the presence of a 6 / isopropyl alcohol solution. The resulting reaction mixture is distilled under vacuum, 1,1,3,3,6,6-hexachloro-1,3,6- Trisilaheptane and 2,2,5,5,7,7,1 An organosilicon compound such as 0,10-octachloro-2,5,7,10-tetrasilaundecane is obtained. These organosilicon compounds are useful as intermediates for producing silicon carbide by a pyrolysis method.
priorityDate 1999-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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