Organocatalytic Imidazolium Ionic Liquids H/D Exchange Catalysts

Author(s)

Zanatta, Marcileia ; dos Santos, Francisco P. ; Biehl, Cristina ; Marin, Graciane ; Ebeling, Gunter ; Netz, Paulo A. ; Dupont, Jairton

• Document type: Journal article
• Source: Journal of Organic Chemistry; v. 82, n. 5, p. 2622-2629, MAR 3 2017.
• Web of Science Citations: 6

Abstract

Simple 1,2,3-trialkylimidazolium cation associated with basic anions, such as hydrogen carbonate, prolinate, and imidazolate, is an active catalyst for the H/D exchange reaction of various substrates using CDCl3 as D source, without the addition of any extra bases or metal. High deuterium incorporation (up to 49%) in acidic C-H bonds of ketone and alkyne substrates (pK(a) from 18.7 to 28.8) was found at room temperature. The reaction proceeds through the fast and reversible deuteration of the 2-methyl H of the imidazolium cation followed by D transfer to the substrate. The IL acts as a neutral base catalyst in which the contact ion pair is maintained in the course of the reaction. The basic active site is due to the presence of a remote basic site in the anion namely, OH of bicarbonate, NH of prolinate, and activated water in the imidazolate anion. Detailed kinetic experiments demonstrate that the reaction is first order on the substrate and pseudozero order relative to the ionic liquid, due to the fast reversible reaction involving the deuteration of the ionic liquid by the solvent. (AU)

• FAPESP's process: 15/08541-6 - Nuclear magnetic resonance spectroscopy: beyond molecular structure assignment
• Grantee: Claudio Francisco Tormena
• Support Opportunities: Research Projects - Thematic Grants