Facile synthesis of a chiral ionic liquid derived from 1-Phenylethylamine
journal contribution
posted on 2024-11-16, 06:20authored bySyed Ashraf, Gordon WallaceGordon Wallace, Leon Kane-Maguire, Yingpit Pornputtkul
A simple route is described to enantiomerically pure ionic liquids derived from (+)- and (–)-1-phenylethylamine. These very low melting point (–42°C) ionic liquids, containing the bis(trifluoromethylsulfonylimide) anion, possess a wide electrochemical potential window between –2.0 and +2.0 V (versus Ag|AgCl). They show chiral discrimination between the enantiomeric forms of Mosher’s salt, suggesting their potential as media for electrochemical asymmetric syntheses or chiral chromatography.
Ashraf, S. A., Pornputtkul, Y., Kane-Maguire, L. A. & Wallace, G. G. (2007). Facile synthesis of a chiral ionic liquid derived from 1-Phenylethylamine. Australian Journal of Chemistry: an international journal for chemical science, 60 64-67.