No Transition Metals Required – Oxygen Promoted Synthesis of Imines from Primary Alcohols and Amines under Ambient Conditions

The synthesis of imines denotes a cornerstone in organic chemistry. The use of alcohols as renewable substituents for carbonyl‐functionality represents an attractive opportunity. Consequently, carbonyl moieties can be in situ generated from alcohols upon transition‐metal catalysis under inert atmosphere. Alternatively, bases can be utilized under aerobic conditions. In this context, we report the synthesis of imines from benzyl alcohols and anilines, promoted by KOtBu under aerobic conditions at room temperature, in the absence of any transition‐metal catalyst. A detailed investigation of the radical mechanism of the underlying reaction is presented. This reveals a complex reaction network fully supporting the experimental findings. Transition‐metal free: The synthesis of imines from benzyl alcohol and anilines promoted by oxygen and KOtBu at room temperature in the absence of a transition metal catalyst is described. The detailed investigation of the radical mechanism is presented revealing complex reaction paths and branching patterns.