Directing-Group-Free Arene C(sp2)–H Amination Using Bulky Aminium Radicals and DFT Analysis of Regioselectivity

A hydroxylamine-derived electrophilic aminating reagent produces a transient and bulky aminium radical intermediate upon in situ activation by either TMSOTf or TFA and a subsequent electron transfer from an iron­(II) catalyst. Density functional theory calculations were used to examine the regioselectivity of arene C–H amination reactions on diversely substituted arenes. The calculations suggest a simple charge-controlled regioselectivity model that enables prediction of the major C­(sp2)–H amination product.