Synthesis 2022; 54(20): 4481-4494
DOI: 10.1055/a-1883-1357
paper

Carbon Chain Rupture: Base-Induced Radical C–C Bond Cleavage of Alkylbenzimidazoles

Xuegang Fu
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Dongyang Guo
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Yuting Yan
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Timotius Marselo
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Mingyu Zhang
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Zhenghan Zhang
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Siying Li
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
,
Jianhui Huang
a   School of Pharmaceutical Science and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. of China
b   Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin 300072, P. R. of China
c   Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency, P. R. of China
› Institutsangaben

This work was funded by the National Natural Science Foundation of China (Grant Nos. 21672159, 21871207).


Abstract

A base-mediated aerobic oxidation of alkylbenzimidazoles for the preparation of carboxylic acids is described. A number of aliphatic carboxylic acids have been prepared in good to excellent yields via a C–C bond rupture process. Preliminary mechanistic studies suggest the reaction undergoes a radical pathway initiated by strong bases such as potassium amide. This type of transformation provides an alternative strategy for the access of important carboxylic acid moieties.

Supporting Information



Publikationsverlauf

Eingereicht: 03. April 2022

Angenommen nach Revision: 23. Juni 2022

Accepted Manuscript online:
23. Juni 2022

Artikel online veröffentlicht:
27. Juli 2022

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