1. Centre of Advanced Studies, Department of Chemistry, University of Rajasthan, Jaipur 302 004, India;2. Department of Chemistry, Malaviya National Institute of Technology, Jaipur 302 017, India
Abstract:
A ‘one pot’ synthesis of 2‐aryl‐4H‐1‐benzopyran‐4‐ones (3a‐3f) is being reported. A mixture of o‐hydroxyacetophenone, aroyl chloride, powdered n‐tetrabutylammonium hydrogensulphate (n‐TBAHSO4) and potassium hydroxide (KOH) were either irradiated by microwaves or sonicated in an ultrasonic cleaning bath to afford flavones directly. On the contrary, conventional liquid‐liquid Phase Transfer Catalysis (PTC) using benzene as organic phase and aqueous KOH as the second phase afforded first β‐diketones in accordance with Baker‐Venkataraman synthesis which upon cyclization by p‐toluenesulphonic acid (p‐TSA) gave desired flavones in the next step. PTC coupled with microwaves or ultrasound show enhanced yields, the clean reaction conditions require less time, and have easier workup protocol. All synthesized compounds were characterized by their Proton Magnetic Resonance (PMR), IR, FAB Mass and elemental analyses.
