Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst

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Abstract

In this work, we report the use of bulk and silica-supported Wells-Dawson acid (H2P2W18O62.24H2O) as reusable, heterogeneous catalysts to obtain substituted flavones and chromones for the cyclization of 1-(2-hydroxyphenyl)-3-aryl-1,3-propanediones. The reaction experiments were performed using toluene as solvent at reflux and in the absence of solvent, at 110°C. Under these conditions eleven examples were obtained with very good yields (82-91%) and high selectivity. The catalysts were easily recycled and reused without loss of their catalytic activity. The presented synthetic method is a simple, clean and environmentally friendly alternative for synthesizing substituted flavones and chromones. ©ARKAT USA, Inc.

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Bennardi, D. O., Romanelli, G. P., Jios, J. L., Autino, J. C., Baronetti, G. T., & Thomas, H. J. (2008). Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst. Arkivoc, 2008(11), 123–130. https://doi.org/10.3998/ark.5550190.0009.b12

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