Catalysis‐Controlled Selective N‐mono or N‐di‐methylation of Anilines: A Review on Synthesis of N‐methyl or N,N‐dimethyl anilines

Author:

Zhang Fuhua1,Chen Kun1,Min Xin123,Yang Wen123,Su Miaodong4,Cao Zhongzhong123ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering Jiujiang University Jiujiang 332005 China

2. Jiangxi Province Engineering Research Center of Ecological Chemical Industry Jiujiang University Jiujiang 332005 China

3. Jiujiang Key Laboratory of Organosilicon Chemistry and Application Jiujiang 332005 China

4. Hunan Huateng Pharmaceutical Co. LTD Changsha 410082 China

Abstract

AbstractN‐alkyl anilines are a series of common and versatile compounds which not only have been used as reaction solvents, acid‐accepters, and organic‐bases, but also in synthesis of dyes, pharmaceuticals, and anti‐colodal. The N‐methyl and/or N,N‐dimethyl anilines are the most representative ones among these. Due to their widespread uses, numerous works have been reported on synthetic strategies in the past decades. The studies on N−H methylations of anilines mainly focus on selection of reagents, selection of catalysts, or ligands design. Different transition‐metals, e. g., Ir, Ru, Pd, and et. al, with different ligands have been used in the methylation protocols. Methanol (CH3OH), carbon dioxide (CO2), formaldehyde (HCHO), or dimethyl carbonate ((CH3)2CO3) was used as C source, and hydrogen (H2) or silanes as H source. In this work, we would like to summarize the latest advances on the synthesis of N‐methyl (N,N‐dimethyl included) anilines and derivatives. This review provides an overview of reactants and catalyst, as well as an emphasis on the scope of substrates and proposed reaction mechanism for each work.

Publisher

Wiley

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