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Double-Carrousel Mechanism for Mn-Catalyzed Dehydrogenative Amide Synthesis from Alcohols and Amines

2021; American Chemical Society; Volume: 11; Issue: 10 Linguagem: Inglês

10.1021/acscatal.1c00693

2155-5435

Jesús Antonio Luque‐Urrutia, Tània Pèlachs, Miquel Solà, Albert Poater,

Carbon dioxide utilization in catalysis

We study with density functional theory calculations the mechanism of the original example of a base-metal-catalyzed synthesis of amides from alcohols and amines. A preliminary proposal of the mechanism of this reaction was experimentally reported by Milstein and co-workers. Instead of the proposed reaction mechanism with a hemilabile pincer amine arm, our DFT calculations describe a facile protocol, where the catalyst only produces aldehydes from alcohols. Once formaldehyde is formed from methanol, it reacts with the amine to form a second alcohol. This new alcohol undergoes the same procedure as methanol and creates the desired amide through a double-carrousel mechanism. The rate-determining step in the catalytic aldehyde synthesis corresponds to the H2 formation. However, in the nonmetal-catalyzed part of the mechanism, the interaction of formaldehyde with the amine is also quite kinetically demanding.