Geminal Brønsted acid ionic liquids as catalysts for the Mannich reaction in water

Int J Mol Sci. 2014 May 15;15(5):8656-66. doi: 10.3390/ijms15058656.

Abstract

Quaternary ammonium geminal Brønsted acid ionic liquids (GBAILs) based on zwitterionic 1,2-bis[N-methyl-N-(3-sulfopropyl)-alkylammonium]ethane (where the carbon number of the alkyl chain is 4, 8, 10, 12, 14, 16, or 18) and p-toluenesulfonic acid monohydrate were synthesized. The catalytic ionic liquids were applied in three-component Mannich reactions with an aldehyde, ketone, and amine at 25 °C in water. The effects of the type and amount of catalyst and reaction time as well as the scope of the reaction were investigated. Results showed that GBAIL-C14 has excellent catalytic activity and fair reusability. The catalytic procedure was simple, and the catalyst could be recycled seven times via a simple separation process without noticeable decreases in catalytic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acids / chemistry*
  • Aldehydes / chemistry
  • Amines / chemistry
  • Benzenesulfonates / chemical synthesis
  • Benzenesulfonates / chemistry
  • Catalysis
  • Ionic Liquids / chemistry*
  • Ketones / chemistry
  • Mannich Bases / chemistry*
  • Quaternary Ammonium Compounds / chemistry
  • Water / chemistry*

Substances

  • Acids
  • Aldehydes
  • Amines
  • Benzenesulfonates
  • Ionic Liquids
  • Ketones
  • Mannich Bases
  • Quaternary Ammonium Compounds
  • Water
  • 4-toluenesulfonic acid