http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1060898-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e2ea8919ae1840f418f59f60e2531123 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-14 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C319-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C327-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F36-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F36-04 |
| filingDate | 1966-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6084851aea6f995a9ca520f79f86b2b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75ee5223657c8a546bd36a9c24b3a740 |
| publicationDate | 1967-03-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1060898-A |
| titleOfInvention | Methods of making primary mercaptans |
| abstract | Primary mercaptans are prepared by reacting terminal olefins with thiol-carboxylic acids (up to C7), followed by hydrolysis of the "antiMarkownikoff" ester product. An initiator such as azo-bisisobutyronitrile may be used for the addition reaction. Exemplified primary mercaptans prepared by hydrolysing the intermediate acetyl compounds (from the appropriate olefins and thiolacetic acid) are: n-dodecyl, 2-ethylhexyl, C11- 15 mixed alkyl, 2-phenylethyl, n-octyl, eicosyl, n-hexyl, cyclohexyl and C15- 20 mixed alkyl. |
| priorityDate | 1966-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.