Pd-catalyzed ethylene methoxycarbonylation with Brønsted acid ionic liquids as promoter and phase-separable reaction media

  • Eduardo J. García-Suárez
  • , Santosh G. Khokarale
  • , Olivier N. Van Buu
  • , Rasmus Fehrmann
  • , Anders Riisager*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

60 Citations (Scopus)

Abstract

Brønsted acid ionic liquids (BAILs) were prepared and applied as combined acid promoters and reaction media in Pd-phosphine catalyzed methoxycarbonylation of ethylene to produce methyl propionate. The BAILs served as alternatives to common mineral acids required for the reaction, e.g. methanesulfonic acid or sulfuric acid, resulting in high catalytic activity and selectivity towards methyl propionate. In addition, the BAILs yielded a biphasic system with the product and provided stability to palladium intermediates avoiding the undesirable formation of palladium black after reaction. These special features enabled facile methyl propionate separation and recovery of the ionic liquid catalyst system, thus allowing its re-use up to 15 times without apparent loss of catalytic activity or selectivity.

Original languageEnglish
Pages (from-to)161-166
Number of pages6
JournalGreen Chemistry
Volume16
Issue number1
DOIs
Publication statusPublished - Jan 2014
Externally publishedYes

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