ABSTRACT
The mixed-ligand system NiCl(2)(dppp)/dppf is shown to be an effective catalyst for the neopentylglycolborylation of ortho-, meta-, and para-substituted electron-rich and electron-deficient aryl mesylates and tosylates. The addition of Zn powder as a reductant dramatically increases the reaction yield and reduces the reaction time by more than an order of magnitude, providing complete conversion in 1-3 h.
Subject(s)
Boronic Acids/chemistry , Mesylates/chemistry , Nickel/chemistry , Tosyl Compounds/chemistry , Zinc/chemistry , Catalysis , Ligands , Organometallic Compounds/chemistryABSTRACT
The mixed ligand system 10 mol % NiCl(2)(dppp) with 5 mol % dppf was discovered to be an extremely efficient catalyst for the neopentylglycolborylation of a diversity of electron-rich and electron-deficient aryl chlorides. Optimization showed that 5 mol % catalyst with 10% dppf was even more efficient. These results highlight the complexity of the relationship between catalyst and coligand in Ni catalysis and the benefit of combinations of mixed ligand in catalyst design.