The Suzuki Reaction in Aqueous Media Promoted by P, N Ligands

The synthesis and structure of palladium complexes of trisubstituted PTA derivatives, PTA(R3), are described. Water-soluble phosphine ligands 1,3,5-triaza-7-phosphaadmantane (PTA), tris(aminomethyl)phosphine trihydrobromide, tri(aminomethyl)phosphine, 3,7-dimethyl-1,5,7-triaza-3-phosphabicyclo[3,3,1]nonane (RO-PTA), 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (DAPTA), lithium 1,3,5-triaza-7phosphaadamantane-6-carboxylate (PTA-CO(2)Li), 2,4,6-triphenyl-1,3,5-triaza-7-phosphatricyclo [3.3.1.1]decane, and 2,4,6-triphenyl-1,3,5-triaza-7-phosphatricyclo[3.3.1.1] decane were used as ligands for palladium catalyzed Suzuki reactions in aqueous media. RO-PTA in combination with palladium acetate or palladium chloride was the most active catalyst for Suzuki cross coupling of aryl bromides and phenylboronic acid at 80 degrees C in 1:1 water: acetonitrile. The activity of Pd(II) complexes of RO-PTA is comparable to PPh(2)(m-C(6)H(4)SO(3)Na) (TPPMS) and P(m-C(6)H(4)SO(3)Na)(3) (TPPTS) and less active than tri(4,6-dimethyl-3-sulfonatophenyl) phosphine trisodium salt (TXPTS). Activated, deactivated, and sterically hindered aryl bromides were examined, with yields ranging from 50% to 90% in 6 h with 5% palladium precatalyst loading. X-ray crystal structures of (RO-PTA)PdCl(2), (PTA(R3))(2)PdCl(2) (R = Ph, p-tert-butylC(6)H(5)), and PTA(R3) (R = p-tert-butylC(6)H(5)) are reported.