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South African Journal of Chemistry

versão On-line ISSN 1996-840X

Resumo

RAFIEE, Ezzat; MAHDAVI, Houri  e  JOSHAGHANI, Mohammad. Iodination of alcohols over Keggin-type heteropoly compounds: A simple, selective and expedient method for the synthesis of alkyl lodides. S.Afr.j.chem. (Online) [online]. 2010, vol.63, pp. 135-140. ISSN 1996-840X.

Different catalysts derived from Keggin-type heteropoly compounds were prepared and their catalytic activities have been compared in the iodination of benzyl alcohol with KI under mild reaction conditions. A high catalytic activity was found over tungstophosphoric acid supported on silica and titania. The effect of catalyst loading, iodine source and the nature of substituents on the aromatic ring of benzyl alcohol were investigated. Finally, several competitive reactions were studied between structurally diverse alcohols. This protocol provides a mild and expedient way for the conversion of various alcohols to their corresponding alkyl iodides with high selectivity.

Palavras-chave : Keggin-type heteropoly compounds; supported catalyst; alcohols; alkyl iodides; potassium iodide.

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