Selective hydroboration of electron-rich isocyanates by an NHC-copper(i) alkoxide

Abstract

The (IPr)CuOtBu catalysed reduction of 11 aryl and alkyl isocyanates with pinacolborane gave only the boraformamides, pinBN(R)C(O)H, in most cases. Overreduction, which hampers almost all isocyanate hydroborations, was restricted to electron poor aryl isocyanates (4-NC-C₆H₄NCO, 4-F₃C-C₆H₄NCO, 3-O₂N-C₆H₄NCO). Computational analysis showed stability of [(IPr)CuH]₂, which was proposed to be the catalyst resting state, drives selectivity, suggesting an approach to prevent overreduction in future work. In the case of iPrNCO, formation of this species renders overreduction kinetically inaccessible. For 4-NC-C₆H₄NCO, however, the barrier height for the first step of over-reduction is much lower, even relative to [(IPr)CuH]₂, resulting in unselective reduction.