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South African Journal of Chemistry

versión On-line ISSN 1996-840X
versión impresa ISSN 0379-4350


RAFIEE, Ezzat; NEJAD, Fereshteh Khajooei  y  JOSHAGHANI, Mohammad. Solventless synthesis of quinoline derivatives: Acceleration of Friedländer reaction by supported heteropoly acids. S.Afr.j.chem. (Online) [online]. 2011, vol.64, pp.95-100. ISSN 1996-840X.

Different Keggin type heteropoly acids (HPAs) and supported ones on solids with different nature and textural properties were used in the Friedländer reaction in order to obtain quinoline derivatives. This conversion has been preceded by tungstophosphoric acid supported on silica, KSF and activated carbon as optimized catalysts in high yields and short reaction times. The general applicability of this method is demonstrated by using various substrates including ketones, β-ketoesters and β-diketones. For most substrates the reaction worked well. These catalysts were found to be reusable and considerable catalytic activity could still be achieved after the fourth run.

Palabras clave : Friedländer reaction; quinoline derivatives; heteropoly compound; supported catalysts; solvent-free condition.

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