Reductive Synthesis of Alcohols from Carboxylic Acids and Esters Catalyzed by a Copper N-heterocyclic Carbene Complex

Hui Zhou , Nana Wei , Zhiqiang Ren , Haojie Ma , Yuqi Zhang , Bo Han

Chinese Journal of Chemistry ›› 2025, Vol. 43 ›› Issue (1) : 73 -78.

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Chinese Journal of Chemistry ›› 2025, Vol. 43 ›› Issue (1) : 73 -78. DOI: 10.1002/cjoc.202400766
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Reductive Synthesis of Alcohols from Carboxylic Acids and Esters Catalyzed by a Copper N-heterocyclic Carbene Complex

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Abstract

Comprehensive Summary:The present work prepared a copper N-heterocyclic carbene complex that could be used in catalyzing the homogeneous hydrogenation of carboxylic acid with ammonia borane (hydrogen source) to synthesize primary alcohols. Various aromatic and aliphatic carboxylic acids with diverse functional groups were transformed to respective alcohols in moderate to high yields. The process can be easily scaled up (TON up to 14545) and exhibits a high compatibility with different sensitive functional groups, including fluorine, chlorine, bromine, iodine, hydroxyl, cyano and nitro groups. IMesCuCl/NH 3·BH 3 combination can selectively reduce aromatic and aliphatic esters. Mechanistic studies indicate that Cu-H species produced in situ are the active intermediates.

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Homogeneous / Reduction / Copper / Carboxylic acids / Esters

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Hui Zhou, Nana Wei, Zhiqiang Ren, Haojie Ma, Yuqi Zhang, Bo Han. Reductive Synthesis of Alcohols from Carboxylic Acids and Esters Catalyzed by a Copper N-heterocyclic Carbene Complex. Chinese Journal of Chemistry, 2025, 43(1): 73-78 DOI:10.1002/cjoc.202400766

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