BBr<sub>3</sub>-Mediated <i>ortho</i> C–H Borylation of Benzamides

We have developed a BBr<sub>3</sub>-mediated, metal-free <i>ortho</i> C-H borylation of benzamides, enabling the synthesis of a wide range of <i>ortho</i>-borylated benzamides in moderate to good yields. This transformation offers a convenient strategy for accessing functionalized benzamides, which are valuable intermediates in pharmaceuticals, agrochemicals, and fine chemical synthesis.

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Publication Details

Journal
Organic Letters
Published
2025-04-25
DOI
https://doi.org/10.1021/acs.orglett.5c00822
Citations
8
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
7.49

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article

BBr3-Mediated ortho C–H Borylation of Benzamides

C. Dong, Yijia Xu, Jingrong Cao, Hua Zhang et al.
8 citations
Organic Letters
Catalytic C–H Functionalization Methods
7.49
article

BBr3-Mediated ortho C–H Borylation of Benzamides

C. Dong, Yijia Xu, Jingrong Cao, Hua Zhang, Yixuan Liang, Chengyu Du
article en
8 citations

Abstract

We have developed a BBr<sub>3</sub>-mediated, metal-free <i>ortho</i> C-H borylation of benzamides, enabling the synthesis of a wide range of <i>ortho</i>-borylated benzamides in moderate to good yields. This transformation offers a convenient strategy for accessing functionalized benzamides, which are valuable intermediates in pharmaceuticals, agrochemicals, and fine chemical synthesis.

Organic LettersVol. 27(18)
Minzu University of China (CN)
National Natural Science Foundation of China, South-Central University for Nationalities
Openalex Percentile: Top 3%
Catalytic C–H Functionalization Methods
7.49
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