Issue 35, 2019

The α-alkylation of ketones with alcohols in pure water catalyzed by a water-soluble Cp*Ir complex bearing a functional ligand

Abstract

A water-soluble dinuclear Cp*Ir complex bearing 4,4′,6,6′-tetrahydroxy-2,2′-bipyrimidine as a bridging ligand was found to be a highly effective catalyst for the α-alkylation of ketones with alcohols in pure water. In the presence of catalyst (0.5 mol%), a series of desirable products were obtained with high reaction economy under environmentally benign conditions. The importance of the hydroxy group in the ligand for catalytic hydrogen transfer was confirmed by mechanism experiments. Furthermore, the application of this catalytic system for the synthesis of a biologically active molecule donepezil in pure water has been accomplished. Notably, this research would facilitate the progress of C–C bond-forming reactions in water catalyzed by water-soluble metal–ligand bifunctional catalysts.

Graphical abstract: The α-alkylation of ketones with alcohols in pure water catalyzed by a water-soluble Cp*Ir complex bearing a functional ligand

Supplementary files

Article information

Article type
Paper
Submitted
27 Jun 2019
Accepted
08 Aug 2019
First published
09 Aug 2019

New J. Chem., 2019,43, 14057-14065

The α-alkylation of ketones with alcohols in pure water catalyzed by a water-soluble Cp*Ir complex bearing a functional ligand

C. Meng, J. Xu, Y. Tang, Y. Ai and F. Li, New J. Chem., 2019, 43, 14057 DOI: 10.1039/C9NJ03345A

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