Ionic liquid catalysed synthesis of β-hydroxy ketones

Sanjib Kumar Karmee, Ulf Hanefeld*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

Abstract

Different acidic ionic liquids (ILs; namely, 1-methylimidazolium tetrafluoroborate, 1-methylimidazolium trifluoroacetate, N-methyl-2-pyrrolidone hydrogen sulfate, N,N,N-trioctyl-n-butanesulfonic acid ammonium hydrogen sulfate, 1-methyl-3-(3-sulfobutyl)imidazolium hydrogen sulfate) and basic ILs (namely, 1,1,3,3-tetramethylguanidinium lactate and choline hydroxide) were tested as catalysts for the aldol reaction. The choline hydroxide catalysed reaction gave high yield (94.3%) and selectivity of the 4-hydroxy-4-phenylbutan- 2-one after a short reaction time (15min) at 0°C. This article demonstrates the potential of choline hydroxide, which is a derivative of choline and a naturally occurring water-soluble essential nutrient, as a highly active and selective green catalyst.

Original languageEnglish
Pages (from-to)1118-1123
JournalChemSusChem (Print): chemistry & sustainability, energy & materials
Volume4
Issue number8
DOIs
Publication statusPublished - 2011

Keywords

  • aldol reaction
  • ionic liquids
  • organocatalysis
  • sustainable chemistry

Fingerprint

Dive into the research topics of 'Ionic liquid catalysed synthesis of β-hydroxy ketones'. Together they form a unique fingerprint.

Cite this