Aqueous reaction and processing in Suzuki-Miyaura couplings using immobilized palladium catalysts in a phosphine-free system

ACSAICHE 99093

Peter Styring, p.styring@sheffield.ac.uk and Nam TS. Phan. Department of Chemical & Process Engineering, The University of Sheffield, Mappin Street, Sheffield, S1 3JD, United Kingdom

A holistic process approach to the Suzuki-Miyaura coupling is reported using an essentially water based system containing only 3% toluene in the initial reaction mixture.  The base was chosen to be soluble in water and the temperature was maintained at 90 °C under stirred batch conditions.

A reactive crystallization process occurs where the product precipitated as a fine white powder.  By tuning the ratio of boronic acid to organobromide we were able to drive the reaction to 100% yield of product with 100% selectivity.  The solid phase catalyst was filtered off using a coarse mesh and washed with 0.1M aqueous sodium hydroxide followed by water.  The fine crystalline product was recovered by filtration through a porous frit.  Analysis of the product showed it to be free from contamination.  Excess reagents were then recycled back into the reaction.  Results using a diverse range of boronic acids and organobromides will be reported.