Reductive transformations of organofluorine compounds: II. Hydrodechlorination of chloropolyfluoroarenes by the action of zinc Full article
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Russian Journal of Organic Chemistry
ISSN: 1070-4280 , E-ISSN: 1608-3393 |
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| Output data | Year: 2000, Volume: 36, Number: 10, Pages: 1488-1499 Pages count : 12 | ||
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Abstract:
Polyfluoroarenes containing chlorine atoms in the aromatic ring and/or in the benzylic position undergo hydrodechlorination by the action of zinc in aqueous dimethylformamide. The use of Zn/Cu and addition of salts (NaCl, Na2SO4, NH4Cl) favor reductive dechlorination of the Carom - Cl bond. Polyfluorobenzotrichlorides react with excess zinc to give the corresponding CH3-substituted derivatives, otherwise CH2Cl- and CHCl2-containing compounds are formed. The reduction of C6F5CCl3 and C6F5CH2Cl with zinc in the presence of copper provides lower yields of the hydrodechlorination products and leads to formation of 1,2-bis(pentafluorophenyl)ethane.
Cite:
Krasnov V.I.
, Platonov V.E.
Reductive transformations of organofluorine compounds: II. Hydrodechlorination of chloropolyfluoroarenes by the action of zinc
Russian Journal of Organic Chemistry. 2000. V.36. N10. P.1488-1499. WOS Scopus РИНЦ
Reductive transformations of organofluorine compounds: II. Hydrodechlorination of chloropolyfluoroarenes by the action of zinc
Russian Journal of Organic Chemistry. 2000. V.36. N10. P.1488-1499. WOS Scopus РИНЦ
Identifiers:
| Web of science: | WOS:000168062000013 |
| Scopus: | 2-s2.0-0034287305 |
| Elibrary: | 13352492 |