A Biphasic Medium Slows Down the Transfer Hydrogenation and Allows a Selective Catalytic Deuterium Labeling of Amines from Imines Mediated by a Ru−H/D + Exchange in D 2 O

The transfer hydrogenation (TH) of several aldimines has been studied using [RuCl(p-cymene)(dmbpy)]BF4, 1, (dmbpy=4,4'-dimethyl-2,2-bipyridine) as a precatalyst. Both neat water and a biphasic water/toluene mixture (w/t) have been successfully used as solvents. In the w/t medium the corresponding precursors, amine and aldehyde, were also used as substrates for a transfer hydrogenative reductive amination. Selective deuterium labeling of the resulting alkylated amines was the main goal of this work. On using D2O the D-content in the amine was negligible but a high level of D-incorporation was achieved in D2O/toluene. According to calculations, this is due to the effect of the relative rates of the hydride transfer and that of the RuH/D+ exchange. The incorporation of deuterium increases with time as a consequence of the reduction in the hydride transfer rate as the substrate concentration diminishes. The recyclability assays performed reflect the importance of pH in the selectivity of the TH towards the imine or the aldehyde resulting from imine hydrolysis.