TEMPO-Promoted Mono- and Bisimidation of Tertiary Anilines: Synthesis of Symmetric and Unsymmetric -Mannich Bases.

A TEMPO-promoted method was developed for the synthesis of symmetric bis--Mannich bases via sequential activation of two α,α'-amino C(sp)-H bonds of ,-dimethylanilines under mild conditions. This methodology was further extended for monoimidation of α-amino-functionalized methylanilines to give unsymmetric -Mannich bases in good to high yields. Several control experiments were performed, and the coupling reaction outcomes indicated that the oxoammonium (TEMPO) species is involved in the reaction.