Indonesian Journal of Chemistry (Nov 2011)

SYNTHESIS 7-HYDROXY-3’,4’-DIMETHOXYISOFLAVON FROM EUGENOL

  • Andi Hairil Alimuddin,
  • Muhammad Idham Darussalam Mardjan,
  • Sabirin Matsjeh,
  • Chairil Anwar,
  • Mustofa Mustofa,
  • Eti Nurwening Sholikhah

DOI
https://doi.org/10.22146/ijc.21404
Journal volume & issue
Vol. 11, no. 2
pp. 163 – 168

Abstract

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Eugenol from the isolation of clove leaves oil had been utilized in the synthesis of 7-hydroxy-3',4'-dimethoxy-isoflavone based on deoxybenzoin intermediate. The raw material was firstly converted into methyleugenol using DMS (89.87%). Secondly, methyl eugenol was oxidized using KMnO4 to produce 3,4-dimethoxybenzyl carboxylic acid (21%). Friedel-Craft acylation of it with recorcinol produced 3,4-dimethoxybenzyl-2',4'-dihydroxyphenyl ketone (deoxybenzoin intermediate) in 78% yield. Eventually, cyclization of the intermediate with reagents of BF3.OEt2/DMF/POCl3 yielded 7-hydroxy-3',4'-isoflavone in 85% yield.

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