A novel efficient protocol for preparation of 3-formyl-2-arylbenzo[b]furan derivatives

  • Benren Liao
  • , Libo Ruan
  • , Min Shi
  • , Nian Li
  • , Liang Chang
  • , Leping Liu
  • , Fan Yang*
  • , Jie Tang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

An efficient method for preparation of 3-formyl-2-arylbenzo[b]furan derivatives 4 from 3-chloro-2-(2-methoxyaryl)-1-arylprop-2-en-1-one 2 was developed, and the desired product was obtained in good to excellent yields. By converting 2-(2-methoxyphenyl)-3-oxo-3-phenylpropanal 1 to 2, the regioselectivity problem occurring in the reaction when using 1 as the starting material was successfully avoided. Furthermore, a one-pot procedure for the successive demethylation, cyclization, and hydrolysis was evolved, although the intermediate 3-(dibromomethyl)-2-phenylbenzo[b]furan 3a could be isolated. A plausible mechanism was proposed based on some in situ investigations.

Original languageEnglish
Pages (from-to)3274-3277
Number of pages4
JournalTetrahedron Letters
Volume55
Issue number21
DOIs
StatePublished - 21 May 2014

Keywords

  • 3-Formyl-2-arylbenzo[b]furan
  • Cyclization reaction
  • Demethylation reaction
  • Vinyl chloride

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