http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1018937-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_222971cf9644e5de40cb69922e0b5ebc |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-63 |
| filingDate | 1981-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1983-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ed0e26ef58c0bd25826af286920c4e49 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11475d8989a4df38c9f4a0a4c177d76a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25e76e25c29aca0e2a3a7ba2bea86bdd |
| publicationDate | 1983-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | SU-1018937-A1 |
| titleOfInvention | Process for preparing ethyl esters of alpha-n-fluorobenzyloxy carboxylic acids |
| abstract | SPbSOBB HALF; NII ETHYLON 1X ETHERS-P-CHIGORBENZYLOXYCARVONIUM, 1 ACID. obvdey ffmuly C1% -0-CHR - COOC2H5 where R - alkyd C, -Se or t-CH, CxH. , or CH3PB Nd, o tlicha yu, and by the fact that bromomagnesium alkyl or bromomagnesium aryl is reacted with diethyloxalate in a medium, without diethyl ether and then replacing the solvent with benzene, by means of thermal reductive cleavage of a halogen-mono-etheral ester using an ethereal pro tein et al. and R-HCH (OMdVg) COO CdNuP-fluorobenzyl chloride with a molar ratio of reagents bromomagnesium alkyl (aryl): | diethyl oxalate: p-fluorobenzyl chloride, equal to 1: 1: 1, and the process is conducted at a boiling point. |
| priorityDate | 1981-07-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 32.