Synthesis and Structure of Hypervalent Iodine(III) Reagents Containing Phthalimidate and Application to Oxidative Amination Reactions

A new class of hypervalent iodine reagents containing phthalimidate was synthesized, and structurally characterized by X‐ray analysis. The benziodoxole‐based reagent displays satisfactory solubility in common organic solvents and is reasonably stable in solution as well as in the solid state. The reagent was used for the oxidative amination of the C(sp3)H bond of N,N‐dimethylanilines. In addition, the reagent was also applicable to oxidative amination with rearrangement of trialkylamines as well as enamines that were prepared in situ from secondary amines and aldehydes. Hyper‐active: Benziodoxole‐based hypervalent iodine reagents containing phthalimidate have been prepared and found to be reasonably stable in both the solid and solution states. These reagents resulted in the oxidative amination of C(sp3)H bonds of N,N‐dimethylanilines and were also applicable to an oxidative amination with rearrangement of trialkylamines and of enamines that were prepared in situ from secondary amines and aldehydes.