Transesterification of dimethyl carbonate with phenol using Brønsted and Lewis acidic ionic liquids

Research output: Contribution to journalArticlepeer-review

47 Scopus citations

Abstract

Transesterification reaction of dimethyl carbonate with phenol to methylphenyl carbonate and diphenyl carbonate using dibutyltin oxide catalyst in conjunction with Brønsted and Lewis acidic ionic liquids was studied. It was observed that the use of ionic liquids significantly enhances the yield of diphenyl carbonate. The ionic liquid having p-toluenesulfonate as anion and metal halide (e.g. ZnCl2) as Lewis acid precursor exhibited higher activity and selectivity for diphenyl carbonate formation. Furthermore, the Brønsted and Lewis acidity of ionic liquids was measured by IR spectroscopy using pyridine as a probe and their Lewis acidity order was also determined.

Original languageEnglish
Pages (from-to)207-211
Number of pages5
JournalCatalysis Communications
Volume12
Issue number3
DOIs
StatePublished - 3 Nov 2010
Externally publishedYes

Bibliographical note

Funding Information:
The financial assistance from the Indira Gandhi Center for Atomic Research (IGCAR, India) is kindly acknowledged.

Keywords

  • Brønsted acidic ionic liquids
  • Dimethyl carbonate
  • Diphenyl carbonate
  • Lewis acidic ionic liquids
  • Phenol
  • Transesterification

ASJC Scopus subject areas

  • Catalysis
  • General Chemistry
  • Process Chemistry and Technology

Fingerprint

Dive into the research topics of 'Transesterification of dimethyl carbonate with phenol using Brønsted and Lewis acidic ionic liquids'. Together they form a unique fingerprint.

Cite this