Abstract
We report an earth‐abundant‐metal‐catalyzed double and single methylation of alcohols. A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2‐aminoalcohols can be methylated. Furthermore, alcohol methylation for the synthesis of pharmaceuticals has been demonstrated. The catalyst system tolerates many functional groups among them hydrogenation‐sensitive examples and upscaling is easily achieved. Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K‐Mn catalyst. The catalyst accepts hydrogen as a proton and a hydride from alcohols efficiently and reacts with a chalcone via hydride transfer.
Highlights
We report an earth-abundant-metal-catalyzed double and single methylation of alcohols
A manganese catalyst, which operates at low catalyst loadings and short reaction times, mediates these reactions efficiently
Mechanistic investigations are indicative of a borrowing hydrogen or hydrogen autotransfer mechanism involving a bimetallic K-Mn catalyst
Summary
Abstract: We report an earth-abundant-metal-catalyzed double and single methylation of alcohols. A broad scope of primary and secondary alcohols, including purely aliphatic examples, and 1,2-aminoalcohols can be methylated. The catalyst system tolerates many functional groups among them hydrogenation-sensitive examples and upscaling is achieved.
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