A Dual‐Functional Approach: Temperature‐Dependent Selective N‐Methylation of Amines with Methanol via Skeletal Copper Catalysts

Abstract Selective N‐methylation with green methylating agents is a highly attractive yet challenging topic in organic synthesis and pharmaceutical production. Herein, a skeletal Cu‐based catalyst was developed for the selective N‐methylation of amines using renewable methanol under relatively mild conditions. By simply modulating the reaction temperature, the CuZnAl‐1.5 catalyst enabled tunable synthesis of N‐monomethylated and N,N‐dimethylated amines. A wide range of amines were efficiently methylated in high yields. Kinetic and mechanistic studies revealed a borrowing hydrogen pathway, with N‐monomethylation exhibiting a lower activation energy. The active Cu surface was identified as the key site for methanol activation to form aldehyde intermediate, whose concentration critically influenced product selectivity. The role of Zn in catalyst preparation and catalysis was also elucidated. The catalyst demonstrated excellent applicability in various synthetic scenarios, underscoring the potential of skeletal Cu‐based systems for methylation reaction with methanol.

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Publication Details

Journal
ChemCatChem
Published
2025-03-11
DOI
https://doi.org/10.1002/cctc.202402126
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

A Dual‐Functional Approach: Temperature‐Dependent Selective N‐Methylation of Amines with Methanol via Skeletal Copper Catalysts

Tipeng Wang, Yao Xiao, Yao‐Bing Huang, Qiang Lü et al.
1 links
ChemCatChem
Asymmetric Hydrogenation and Catalysis
article

A Dual‐Functional Approach: Temperature‐Dependent Selective N‐Methylation of Amines with Methanol via Skeletal Copper Catalysts

Tipeng Wang, Yao Xiao, Yao‐Bing Huang, Qiang Lü, Qile Liu, Xuan Zhang, Keming Li, Feng-Shuo Guo
article en

Abstract

Abstract Selective N‐methylation with green methylating agents is a highly attractive yet challenging topic in organic synthesis and pharmaceutical production. Herein, a skeletal Cu‐based catalyst was developed for the selective N‐methylation of amines using renewable methanol under relatively mild conditions. By simply modulating the reaction temperature, the CuZnAl‐1.5 catalyst enabled tunable synthesis of N‐monomethylated and N,N‐dimethylated amines. A wide range of amines were efficiently methylated in high yields. Kinetic and mechanistic studies revealed a borrowing hydrogen pathway, with N‐monomethylation exhibiting a lower activation energy. The active Cu surface was identified as the key site for methanol activation to form aldehyde intermediate, whose concentration critically influenced product selectivity. The role of Zn in catalyst preparation and catalysis was also elucidated. The catalyst demonstrated excellent applicability in various synthetic scenarios, underscoring the potential of skeletal Cu‐based systems for methylation reaction with methanol.

ChemCatChemVol. 17(8)
North China Electric Power University (CN), China Three Gorges Corporation (China) (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 96%
Asymmetric Hydrogenation and Catalysis
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