http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1162557-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6575b65bb924fa9bbd7df085b866d2b1 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C17-08 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C17-08 |
| filingDate | 1966-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_267c2b5264b9143bc4c8f38013068a6f |
| publicationDate | 1969-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1162557-A |
| titleOfInvention | Halogenation of Olefins |
| abstract | 1,162,557. Dibromoalkanes. EL PASO PRODUCTS CO. 14 Oct., 1966, No. 46094/66. Heading C2C. Dibromoalkanes are obtained by introducing anhydrous diolefin and a molar excess of anhydrous hydrogen bromide into a reactor maintained under an anhydrous atmosphere at from - 20‹ to 40‹ C. in the absence of moisture and in the presence of a free-radical initiator. It is preferred to utilize terminal or alpha, omega-diolefins such as 1,3-butadiene, 1,4- pentadiene, 1,5 - hexadiene or 1,6 - heptadiene and the example specifies the hydrobromination of 1,5-hexadiene wherein 1,6-dibromohexane is the main product while 2,5-, 1,4- and 1,5-dibromohexane and 5- and 6-bromohexene-1 are all formed in minor amounts. However any diolefin may be used in the hydrobromination. The free-radical initiator is usually oxygen. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6980959-B1 |
| priorityDate | 1966-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 30.