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Modified Algar-Flynn-Oyamada reaction for the synthesis of 3-hydroxy-2-styryl-chromen-4-ones under solvent-free conditions
Published:
14 November 2022
by MDPI
in The 26th International Electronic Conference on Synthetic Organic Chemistry
session General Organic Synthesis
Abstract:
A simple and efficient condition for Algar-Flynn-Oyamada reaction for the synthesis of 3-hydroxy-2-styryl-chromen-4-ones involving grinding of different 1-(2'-hydroxy-phenyl)-5-aryl-penta-2,4-dien-1-ones with UHP (urea-hydrogen peroxide), pulverized potassium hydroxide and few drops of ethanol at room temperature under solvent-free conditions has been described. A faster reaction and higher yields compared to the conventional methods are the advantages of present protocol. The structure of the synthesised compounds was identified from their spectral data (IR, 1H-NMR).
Keywords: Algar-Flynn-Oyamada reaction; 3-Hydroxy-2-styryl-chromen-4-ones; 1-(2-hydroxy-phenyl)-5-aryl-penta-2,4-dien-1-ones; UHP; solvent-free conditions