http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2007142650-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d245c8f79ec49bc3d07e286b4701a274 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1876 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-08 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 |
| filingDate | 2005-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b01e74b25b668380dbf3cdfe347f211 |
| publicationDate | 2007-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-2007142650-A1 |
| titleOfInvention | Method of making epoxyorganoalkoxysilanes |
| abstract | Epoxyorganoalkoxysilanes are made by reacting an olefin epoxide with an hydridoalkoxysilane in the presence of RhCl(di-tert-butylsulfide) 2 catalyst. The reaction is free of the presence of a stabilizing agent, it is carried out at a temperature in the range of 65-95° C., and the olefin epoxide is present in the reaction in a molar excess of 5-25 percent over the stoichiometric amount necessary to react with the hydridoalkoxysilane. Preferably, the reaction temperature is in the range of 70-75° C., and the olefin epoxide is present in the reaction in a molar excess of about 10 percent over the stoichiometric amount necessary to react with the hydridoalkoxysilane. |
| priorityDate | 2004-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 82.