| Autor: |
Freedman, Bernard, Nelson, Jane, Binder, R., Applewhite, T. |
| Zdroj: |
Journal of the American Oil Chemists' Society (JAOCS); Apr1965, Vol. 42 Issue 4, p340-344, 5p |
| Abstrakt: |
A convenient laboratory preparation of methyl 12-ketostearate is described. Methyl ricinoleate is converted to methyl 12-ketostearate in 70-75% yield by Raney nickel. The type and quantity of Raney nickel have a marked influence on the yield as well as on the time and temp required for the conversion. The reaction is not a direct isomerization as previously assumed but appears to be a two-step process. Methyl ricinoleate is hydrogenated rapidly to methyl 12-hydroxystearate which is then dehydrogenated slowly to the product. Hydrogenolysis of the alcohol function is a competing reaction which is minimized by the proper choice of reaction conditions. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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