http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002534527-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1804 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1888 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18 |
| filingDate | 1999-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2002-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2002534527-A |
| titleOfInvention | Preparation of alkyl (amino) dialkoxysilanes |
| abstract | (57) [Summary]nAn alkyl (amino) dialkoxysilane is prepared by reacting a stoichiometric amount of an alkoxysilane with an alkylaminomagnesium chloride in a reverse addition process under anhydrous conditions. The alkylaminomagnesium chloride is preferably prepared in situ by reacting a Grignard reagent (RMX) with an alkylamine in a suitable aprotic solvent such as tetrahydrofuran. An “alkyl” substituent can be an alkyl, arylalkyl, or aryl. The reaction can be carried out without a catalyst at temperatures in the range of 25-75 ° C, and the aprotic solvent can be recovered and reused in the process. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013155173-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9677178-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9200167-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2008133235-A |
| priorityDate | 1999-01-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 68.