An Efficient Continuous Flow Synthesis for the Preparation of N-Arylhydroxylamines: Via a DMAP-Mediated Hydrogenation Process

被引:3
|
作者
Chen, Jianli [1 ,2 ]
Lin, Xinyu [2 ]
Xu, Feng [3 ]
Chai, Kejie [2 ]
Ren, Minna
Yu, Zhiqun [2 ]
Su, Weike [2 ]
Liu, Fengfan [2 ]
机构
[1] Jiaxing Nanhu Univ, Coll New Mat Engn, Jiaxing 314000, Peoples R China
[2] Zhejiang Univ Technol, Natl Engn Res Ctr Proc Dev Act Pharmaceut Ingredie, Collaborat Innovat Ctr Yangtze River Delta Reg Gre, Hangzhou 310014, Peoples R China
[3] Raybow Hangzhou Pharmaceut Co Ltd, Hangzhou 310014, Peoples R China
来源
MOLECULES | 2023年 / 28卷 / 07期
基金
中国国家自然科学基金;
关键词
N-arylhydroxylamine; 4-(dimethylamino) pyridine; continuous flow; catalytic activity; selectivity; AROMATIC NITRO-COMPOUNDS; SELECTIVE HYDROGENATION; P-AMINOPHENOL; CHEMOSELECTIVE REDUCTION; HYDROXYLAMINES; NITROBENZENE; NITROARENES; CONVERSION; LIGAND; ARYL;
D O I
10.3390/molecules28072968
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The selective hydrogenation of nitroarenes to N-arylhydroxylamines is an important synthetic process in the chemical industry. It is commonly accomplished by using heterogeneous catalytic systems that contain inhibitors, such as DMSO. Herein, DMAP has been identified as a unique additive for increasing hydrogenation activity and product selectivity (up to >99%) under mild conditions in the Pt/C-catalyzed process. Continuous-flow technology has been explored as an efficient approach toward achieving the selective hydrogenation of nitroarenes to N-arylhydroxylamines. The present flow protocol was applied for a vast substrate scope and was found to be compatible with a wide range of functional groups, such as electron-donating groups, carbonyl, and various halogens. Further studies were attempted to show that the improvement in the catalytic activity and selectivity benefited from the dual functions of DMAP; namely, the heterolytic H-2 cleavage and competitive adsorption.
引用
收藏
页数:17
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