Olefin isomerization process

Chemistry of hydrocarbon compounds – Unsaturated compound synthesis – By double-bond-shift isomerization

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585670, 502152, C07C 524, C07C 530

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active

044232764

ABSTRACT:
Internal olefins in the 4 to 30 carbon number range are isomerized to alpha olefins, utilizing cyclopentadienyltantalum compounds in either a catalyst or reagent mode. Under a preferred practice of the process of this invention, internal olefin is contacted with the reagent to form a first complex, alpha olefin is liberated from said first complex upon contact with carbon monoxide to yield a second complex, and reagent is regenerated from said second complex upon contact with water.

REFERENCES:
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patent: 3173967 (1965-03-01), Brown
patent: 3988332 (1976-10-01), Schrock
patent: 4125567 (1978-11-01), Kidwell et al.
Chemical Abstract, 93: 239562a.
McLain et al., J. Am. Chem. Soc., 101(16), 4558, (1979).
J. Schwartz and J. A. Labinger, "Hydrozirconation: A New Transition Metal Reagent . . . ," Angew. Chem. Int. Ed. Engl., 15(1976), p. 333.
A. H. Klazimga and J. H. Teuben, "Synthesis and Properties . . . ," Journal of Organometallic Chemistry, 157(1978), p. 413.

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