Claims
- 1. A process for preparing an internal olefin comprising isomerizing an olefin in the presence of a catalyst comprising a solid base which is obtainable by reacting alumina with an alkali metal hydroxide and an alkali metal hydride or reacting water-containing alumina with an alkali metal hydride in an amount more than the molar equivalent of water contained in the water-containing alumina, at a temperature of 200.degree. to 500.degree. C. in an inert gas atmosphere.
- 2. The process according to claim 1, wherein the solid base is obtainable by reacting alumina with an alkali metal hydroxide and an alkali metal hydride.
- 3. The process according to claim 2, wherein the alumina and the alkali metal hydroxide is reacted at a temperature of 250.degree. to 450.degree. C.
- 4. The process according to claim 2, wherein the alkali metal hydride is reacted with a reaction product of the alumina and the alkali metal hydroxide at a temperature of 250.degree. to 450.degree. C.
- 5. The process according to claim 2, wherein the alkali metal hydroxide is selected from the group consisting of lithium hydroxide, sodium hydroxide, potassium hydroxide, rubidium hydroxide, cesium hydroxide and mixtures thereof.
- 6. The process according to claim 2, wherein the alkali metal hydride is selected from the group consisting of sodium hydride, potassium hydride and lithium hydride.
- 7. The process according to claim 2, wherein an amount of the alkali metal hydroxide is from 5 to 40% by weight based on the weight of alumina.
- 8. The process according to claim 2 wherein an amount of the alkali metal hydride is from 2 to 10% by weight based on the weight of alumina.
- 9. The process according to claim 2, wherein the alumina is selected from the group consisting of .gamma.-alumina, .chi.-alumina, .rho.-alumina and .eta.-alumina and mixtures thereof.
- 10. The process according to claim 1, wherein the solid base is obtainable by reacting a water-containing alumina with an alkali metal hydride.
- 11. The process according to claim 10, wherein the water-containing alumina and the alkali metal hydride is reacted at a temperature of 250.degree. to 450.degree. C.
- 12. The process according to claim 10, wherein the alkali metal hydride is selected from the group consisting of sodium hydride, potassium hydride and lithium hydride.
- 13. The process according to claim 10, wherein the water-containing alumina is reacted with the alkali metal hydride in an amount of 1.01 to 2 time molar equivalents of water contained in the alumina.
- 14. The process according to claim 10, wherein the alkali metal hydride is added in two portions, the first one of which is in an amount not more than a molar equivalent of water contained in the water-containing alumina and the second one of which is the rest of the alkali metal hydride.
- 15. The process according to claim 10, wherein the first portion of the alkali metal hydride is used in an amount of 0.2 to 1 time molar amount of water contained in the alumina.
- 16. The process according to claim 10, wherein the alkali metal hydride is added in one portion and reacted with the water-containing alumina.
- 17. The process according to claim 10, wherein the alumina is one selected from the group consisting of water-containing .gamma.-alumina, .chi.-alumina, .rho.-alumina and .eta.-alumina.
- 18. The process according to claim 10, wherein the water content of the water-containing alumina is 1.2 to 10% by weight.
- 19. The process according to claim 1, wherein the solid base is used in an amount of from 1/2,000 to 1/50 parts by weight per part of the olefin.
- 20. The process according to claim 1, wherein the isomerization temperature is in a range of from -10.degree. to +100.degree. C.
- 21. The process according to claim 1, wherein the olefin to be isomerized is a member selected from the group consisting of 1-butene, 1-pentene, 1-hexene, 1-heptene, 1-nonene, 1-decene, 2-methyl-1-butene, 3-methyl-1-butene, 4-methyl-1-butene, 3-methyl-1-pentene, 2-methyl-1-pentene, 2,3-dimethyl-1-butene, allylbenzene, allyltoluene, 2-isopropenylnorbornane, 5-isopropenyl-2-norbornene, 5-vinyl-2-norbornene, 6-methyl-5-vinylbornene, methylenecyclopentane, methylenecyclohexane, 1,4-pentadiene, 1,5-hexadiene, 2,5-dimethyl-1,4-hexadiene, 2,5-dimethyl-1,5-hexadiene, 4-methyl-2-pentene, and 5-(2-propenyl)-2-norbornene.
Priority Claims (4)
Number |
Date |
Country |
Kind |
62-32790 |
Feb 1987 |
JPX |
|
62-32791 |
Feb 1987 |
JPX |
|
62-32792 |
Feb 1987 |
JPX |
|
62-32793 |
Feb 1987 |
JPX |
|
Parent Case Info
This application is a divisional of copending application Ser. No. 155,848 filed on Feb 16, 1988 now U.S. Pat. No 4,822,764
US Referenced Citations (6)
Divisions (1)
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Number |
Date |
Country |
Parent |
155848 |
Feb 1988 |
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