http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1155579-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6575b65bb924fa9bbd7df085b866d2b1 |
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-582 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2-861 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C2-86 |
filingDate | 1966-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_780ee458a30327e6f010a37dc56bccf8 |
publicationDate | 1969-06-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-1155579-A |
titleOfInvention | Production of Dienes |
abstract | 1,155,579. Diolefins. EL PASO PRODUCTS CO. 14 Oct., 1966, No. 46089/66. Heading C5E. Diolefins are produced by introducing a halide of general formula where R 1 , R 2 , R 3 and R 4 are each hydrogen, alkyl, alkaryl or aralkyl, n is an integer and X is a halogen atom, and an olefin into a reaction zone at 900-1100‹ F. under a pressure of 50- 300 p.s.i.g., allowing the reaction to go to completion and recovering the diolefins produced. The olefin may have up to six carbon atoms. The examples describe the condensation of allyl chloride with propylene to yield 1,5-hexadiene. |
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: 19.