GB865738A - Isomerization of internal olefins - Google Patents
Isomerization of internal olefinsInfo
- Publication number
- GB865738A GB865738A GB8958/59A GB895859A GB865738A GB 865738 A GB865738 A GB 865738A GB 8958/59 A GB8958/59 A GB 8958/59A GB 895859 A GB895859 A GB 895859A GB 865738 A GB865738 A GB 865738A
- Authority
- GB
- United Kingdom
- Prior art keywords
- olefines
- olefine
- hexene
- specified
- boron
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
- C07C1/32—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
- C07C1/321—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a non-metal atom
Abstract
1-Olefines are formed from internal olefines by isomerisation in the presence of an organoboron compound. Suitable conditions are 0-250 DEG C. and up to 150 atmospheres using 0,5-40 mole% of organo-boron compound and a diluent which may be a hydrocarbon, ether, halogen aromatic compound or tertiary amine, many being specified. Specified internal olefines are 2-pentene, 2-butene, 2-hexene, 2-methyl-3-heptene, 3-hexene, 2-octene, 3-octene, 4-decene, 4-octadecene, 2-methylamyl-3-hexene and b -methyl-b -ethyl- or b -isopropylstyrene. The catalyst preferably contains the same number of carbon atoms in the organic radicals present as the olefine to be isomerised and may be formed in situ from diborane and the olefine. Specified catalysts are trimethyl-, thiethyl-, trientyl-, trihexyl-, trioctyl-, tridecyl-, tricyclopentyl-, tricyclohexyl-, and trimethylcyclohexyl-boron, amyl boric acid, diethyl boron bromide, dimethyl diborane, triethylboron-trimethylamine and trioctylboron-triethylamine. Preferably the 1-olefine is distilled off as formed; continuous processes are also possible.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US865738XA | 1958-05-28 | 1958-05-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB865738A true GB865738A (en) | 1961-04-19 |
Family
ID=22199458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB8958/59A Expired GB865738A (en) | 1958-05-28 | 1959-03-16 | Isomerization of internal olefins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB865738A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1468154B1 (en) * | 1963-05-02 | 1972-02-03 | Kuraray Co | Process for the catalytic isomerization of olefin hydrocarbons |
-
1959
- 1959-03-16 GB GB8958/59A patent/GB865738A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1468154B1 (en) * | 1963-05-02 | 1972-02-03 | Kuraray Co | Process for the catalytic isomerization of olefin hydrocarbons |
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