Iodobenzene diacetate (IBD) catalyzed an quick oxidative aromatization of Hantzsch-1,4-dihydropyridines to pyridines under ultrasonic irradiation

Ultrason Sonochem. 2012 Jul;19(4):729-35. doi: 10.1016/j.ultsonch.2011.12.021. Epub 2012 Jan 12.

Abstract

This project was undertaken to demonstrate the potential of iodobenzene diacetate for the oxidative aromatization of Hantzch-1,4-dihydropyridines under ultrasonic irradiation. All reactions were carried out under ultrasonic irradiation and results were compared with traditional method. Sonochemical switching was observed in case of oxidative aromatization of 4-n-alkyl substituted 1,4-DHP. Without sonication, dealkylation occurred in case of n-alkyl substituted 1,4-DHP (ionic mechanism) but under ultrasonic irradiation, n-alkyl group was not expelled (radical mechanism). However, secondary alkyl (isopropyl) and benzyl group were expelled under both conditions.

MeSH terms

  • Acetates / chemistry*
  • Catalysis
  • Iodobenzenes / chemistry*
  • Molecular Structure
  • Oxidation-Reduction
  • Pyridines / chemical synthesis*
  • Pyridines / chemistry
  • Sonication*

Substances

  • Acetates
  • Iodobenzenes
  • Pyridines