Direct Synthesis of Benzothiazoles and Benzoxazoles from Carboxylic Acids Utilizing (<i>o</i>-CF<sub>3</sub>PhO)<sub>3</sub>P as a Coupling Reagent

A general and efficient method for the direct synthesis of benzothiazoles and benzoxazoles from carboxylic acids with 2-aminobenzenethiols or 2-aminophenols using (<i>o</i>-CF<sub>3</sub>PhO)<sub>3</sub>P as a simple coupling reagent has been developed. Diverse benzothiazoles and benzoxazoles were synthesized in moderate to excellent yields. And the gram-scale preparation of benzothiazole and benzoxazole also proceeded smoothly under the mild conditions. Moreover, a plausible reaction mechanism was discussed, with (<i>o</i>-CF<sub>3</sub>PhO)<sub>3</sub>P and its hydrolysis product (<i>o</i>-CF<sub>3</sub>PhO)<sub>2</sub>P(O)H contributing to the formation of the target products as an amide synthesis coupling agent and a cyclization reaction promoter, respectively.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2024-10-25
DOI
https://doi.org/10.1021/acs.joc.4c01807
Citations
6
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.50

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article

Direct Synthesis of Benzothiazoles and Benzoxazoles from Carboxylic Acids Utilizing (o-CF3PhO)3P as a Coupling Reagent

Lin Zhang, Mei Wang, Wenchang Gou, Chun Li et al.
6 citations
The Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.50
article

Direct Synthesis of Benzothiazoles and Benzoxazoles from Carboxylic Acids Utilizing (o-CF3PhO)3P as a Coupling Reagent

Lin Zhang, Mei Wang, Wenchang Gou, Chun Li, Yu Tian, Xuan Zhou, Yunhuan Wang
article en
6 citations

Abstract

A general and efficient method for the direct synthesis of benzothiazoles and benzoxazoles from carboxylic acids with 2-aminobenzenethiols or 2-aminophenols using (<i>o</i>-CF<sub>3</sub>PhO)<sub>3</sub>P as a simple coupling reagent has been developed. Diverse benzothiazoles and benzoxazoles were synthesized in moderate to excellent yields. And the gram-scale preparation of benzothiazole and benzoxazole also proceeded smoothly under the mild conditions. Moreover, a plausible reaction mechanism was discussed, with (<i>o</i>-CF<sub>3</sub>PhO)<sub>3</sub>P and its hydrolysis product (<i>o</i>-CF<sub>3</sub>PhO)<sub>2</sub>P(O)H contributing to the formation of the target products as an amide synthesis coupling agent and a cyclization reaction promoter, respectively.

The Journal of Organic ChemistryVol. 89(22)
Guiyang Medical University (CN)
National Natural Science Foundation of China, Science and Technology Program of Guizhou Province
Clean water and sanitation
Openalex Percentile: Top 19%
Catalytic C–H Functionalization Methods
1.50
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