Abstract

A dioxovanadium complex has been successfully prepared by the reaction of an ONO-donor Schiff base, derived by condensing aminobenzohydrazide and 3-ethoxysalicylaldehyde, with VO2(acac)2. The structures of synthesized products were explored spectroscopically through FT-IR, 1H & 13C NMR, and by elemental composition (CHN) through combustion analysis. The catalytic potential of the complex was explored for the synthesis of substituted quinolines by adapting the Friedländer method. In this method, a cyclocondensation reaction of ortho aminoaryl aldehydes or ketones was carried out with another ketone having an alpha methylene group under solvent-free conditions. The main advantages of the present catalytic work are less time required for the completion of the reaction, high percentage yield, and easy work out procedure.

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