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filingDate 1990-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf18077a89573d7c45660d3455fd52e5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43b07f6f50e2aee2fd0eb414fc813958
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publicationDate 1991-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5071966-A
titleOfInvention Process for preparing an enol silyl ether compound
abstract A process for preparing an enol silyl ether compound from a diazoacetoacetic acid ester having the general formula (IV): ##STR1## wherein R 1 is a lower alkyl group having 1 to 6 carbon atoms, phenyl group, a substituted phenyl group, an aralkyl group or allyl group, and R 2 , R 3 and R 4 are the same or mutually different and each is a lower alkyl group having 1 to 6 carbon atoms, which comprises reacting a diazoacetoacetic acid ester having the general formula (I): ##STR2## wherein R 1 is the same as defined above, with a trialkylsilyl chloride having the general formula (II): ##STR3## wherein R 2 , R 3 and R 4 are the same as defined above, in an inert solvent in the presence of an organic base and an alkali halide having the general formula (III): n n MX (III) n n wherein M is an alkaline metal and X is bromine atom or iodine atom. The desired compound is useful as an intermediate for synthesis of carbapenem β-lactam antibiotics.
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priorityDate 1989-01-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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