Articulo
Synthesis of substituted flavones and chromones using a Wells-Dawson heteropolyacid as catalyst
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Autor
Bennardi, Daniel Oscar
Romanelli, Gustavo Pablo
Jios, Jorge Luis
Autino, Juan Carlos
Baronetti, Graciela Teresita
Thomas, Horacio Jorge
Institución
Resumen
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. Centro de Investigación y Desarrollo en Ciencias Aplicadas Facultad de Ciencias Agrarias y Forestales Laboratorio de Servicios a la Industria y al Sistema Científico