http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-982214-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_73ee0bacab5a7576a6a3244747f6ea99 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C381-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C381-00 |
| filingDate | 1962-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bdc3cbcdfbc36cadb9add752d0347585 |
| publicationDate | 1965-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-982214-A |
| titleOfInvention | Preparation of pentafluorothio-substituted olefines |
| abstract | Compounds of the formula R1R2C : C(R3)SF5, where R1 is hydrogen or chlorine, R2 is hydrogen, alkyl or alkenyl, R3 is hydrogen, or R2 and R3 form a polymethylene chain (cf. 905,006), are prepared by reacting a compound R1R2CCl. CHR3SF5 with an aliphatic primary or secondary amine or a cycloamine under substantially anhydrous conditions. Diethyl ether or a hydrocarbon such as xylene may be used as solvent. An example prepares 2-chlorovinyl sulphur pentafluoride CHCl : CHSF5 from CHCl2 : CH2SF5 and cyclohexylamine; other specified amines are ethylamine, propylamine, butylamine and piperidine. |
| priorityDate | 1962-06-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 34.