http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2586783-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ddb9f3656270bc5410be3679322fead |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-188 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 |
| filingDate | 2011-06-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_440ea1630ec295d635522cd8d18d716d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f29d66673e06b70000d0f8699413264 |
| publicationDate | 2013-05-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-2586783-A1 |
| titleOfInvention | Method for producing alkoxy hydrosilane |
| abstract | Provided is a method for producing an alkoxyhydrosilane, comprising: a reaction (reaction 1) of a halohydrosilane compound (B) represented by H-SiR 2 c (CR 1 3-b Y b ) a X 3-a-c wherein R 1 is a hydrogen atom or C 1-20 hydrocarbon group; R 2 is a C 1-20 hydrocarbon group; X is a halogen atom; Y is a hetero substituent; a is 1 or 2, b is 1, 2 or 3, and c is 1 or 0, provided that a+c is not more than 2, with an alcohol (C) in an amount of 0.50-0.99 molar equivalents relative to Xs of the halohydrosilane compound (B); followed by a reaction (reaction 2) with an orthoester (D) in an amount of 1.00 molar equivalent or more relative to the residual Si-X in the reaction mixture, to produce an alkoxyhydrosilane compound (A) represented by H-SiR 2 c (CR 1 3-b Y b ) a (OR 8 ) 3-a-c wherein R 8 is a C 1-20 hydrocarbon group, and R 1 , R 2 , Y, a, b, and c are as defined above. |
| priorityDate | 2010-06-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 111.