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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-1888
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
filingDate 1997-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2000-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_710c79669a8288b80d1d10902a4b5422
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b98b80e563fa97c9c56d8eaa0eba443
publicationDate 2000-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-6114558-A
titleOfInvention Preparation of alkyl(amino)dialkoxysilanes
abstract Alkyl(amino)dialkoxysilanes are prepared by anhydrously reacting stoichiometric amounts of an alkoxysilane and an alkylaminomagnesium chloride in a reverse addition process. The alkylamino magnesium chloride is preferably prepared in situ by the reaction of a Grignard reagent (RMX) and an alkylamine in a suitable aprotic solvent, such as tetrahydrofuran. The "alkyl" substituent can be alkyl, arylalkyl or aryl. The reaction can be conducted in the temperature range of from 25 DEG C. to 75 DEG C., without a catalyst, and the aprotic solvent is recovered for re-use in the process.
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priorityDate 1997-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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