http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-243578-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1cf48b7f316e5bc4275d9ea603ee700a http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_cf7fc49d7eeaa808175c1206df353dc5 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-42 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-716 |
| filingDate | 1984-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18377e4aa93b0377d78c842575064f0a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_932aae6c4ea78992d386091c54d59b24 |
| publicationDate | 1986-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CS-243578-B1 |
| titleOfInvention | Process for preparing 4-bromo-2- (methoxyimino) -3-oxo-butanoic acid ethyl ester |
| abstract | A method for preparing 4-bromo-2- (methoxyimino) -3-oxobutanoic acid ethyl esternacid is carried outnby reacting 1 mol of the acid ethyl estern2- (methoxyimino) -3-oxobutanoic acid with 0.8 to 1.5nmole of bromine, optionally) proton catalysisnacids, Lewis acids orncomplex Lewis acid compounds.nThe ethyl ester obtained is the preferred intermediatenin the preparation of aminothiazole [beta] -lactamnantibiotics. |
| priorityDate | 1984-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 40.