Partially Fluorinated Aliphatic Compounds by Reductive Desulfurization of Substituted Thiophene
Autor: | H. Gisser, S. Portnoy |
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Rok vydání: | 1962 |
Předmět: | |
Zdroj: | The Journal of Organic Chemistry. 27:3331-3332 |
ISSN: | 1520-6904 0022-3263 |
DOI: | 10.1021/jo01056a518 |
Popis: | The preparation of partially fluorinated organic compounds via reductive desulfurization of appropriately substituted thiophene was investigated. Condensation of a fluoro acid chloride with a thienyl halide was accomplished by a reverse Grignard procedure. Conventional acid condensation techniques did not work. The resulting compound was desulfurized with Raney nickel yielding the aliphatic alcohol and ketone. The alcohol was dehydrated to the olefin and then hydrogenated to the saturated hydrocarbon. The Wolff-Kischner and Clemmensen reduction of the fluorinated ketone were unsuccessful. (Author) |
Databáze: | OpenAIRE |
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