Palladium-catalyzed microwave-assisted Hirao reaction utilizing the excess of the diarylphosphine oxide reagent as the P-ligand; a study on the activity and formation of the “PdP2” catalyst

Abstract

Abstract The microwave-assisted Hirao reaction of bromobenzene and diarylphosphine oxides was performed at 120 °C using triethylamine as the base, and 5% of palladium acetate as the catalyst in ethanol. 5% Excess of the >P(O)H reagent served as the reducing agent, while another 10% as the preligand (in the >POH tautomeric form). It was found that the P–C coupling reaction was significantly faster with (2-MeC6H4)2P(O)H (A) and (3,5-diMeC6H3)2P(O)H (B), than with Ph2P(O)H (C) and (4-MeC6H4)2P(O)H (D). Moreover, species A and B could be applied as selective P-ligands in the reaction of bromobenzene with C or D. Dependence of the effectiveness of “PdP2” catalysts with diarylphosphine oxide preligands on the methyl substituents followed a reversed order as the reactivity of the diarylphosphine oxide species in the P–C coupling itself. Formation of the “PdP2” catalyst from palladium acetate and diarylphosphine oxide has never been studied, but now it was evaluated by us at the B3LYP level of theory applying 6-31G(d,p) for C,H,P,O and SDD/MW28 for Pd including the explicit-implicit solvent model. The novel mechanism requiring three equivalents of the >P(O)H species for each of the palladium acetate molecule was in agreement with the preparative experiments. The ligation of palladium(0) with different P(III) species comprising the >POH form of the >P(O)H reagent was also studied, and the critical role of the steric hindrance on the ligation, and hence on the activity of the “PdP2” catalyst was substantiated. Last but not least, the influence of the Me substituents in the aromatic ring of the P-reagents on the energetics of the elemental steps of the Hirao reaction itself was also evaluated.