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SbCl3-catalyzed solvent-free Friedel–Crafts reaction of phenols with mandelic acids to 3-aryl benzofuran-2(3H)-ones: Synthesis of spirocyclic 2,3-dihydrobenzofuran-2-ones

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Version 2 2016-10-21, 13:19
Version 1 2016-08-30, 07:18
journal contribution
posted on 2016-10-21, 13:19 authored by Bhaskar B. Dhotare, Manoj K. Choudhary, Sandip K. Nayak

A facile, SbCl3-catalyzed, one-pot, tandem Friedel–Crafts/lactonization reaction of phenols and mandelic acids has been developed under solvent-free conditions to afford 3-aryl benzofuran-2(3H)-ones in good to high yields (52–90%). Additionally, the utility of 3-aryl benzofuran-2(3H)-ones is demonstrated by using them as precursors in the synthesis of a new class of spirocyclic benzofuran-2-ones using classical synthetic methodologies.

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