Rapid C–S Coupling in Water via Ion-Pair-Catalyzed Dehydration

The C-S bond is of significant importance due to its unique properties and diverse roles in chemistry, biology, and materials science. In this work, we present an efficient synthetic protocol of a rapidly dehydrative C-S coupling reaction with alcohols and thiols in water catalyzed by a triaryl-carbenium ion pair. Under metal-free conditions, a wide range of thioethers were obtained in good yields (up to 99%) with excellent functional group tolerance, including the fast modification of amino acid derivatives and functional molecules. This method allowed reactions to be conducted with low catalyst loading, down to 1.0 mol %, and was practical for gram-scale synthesis. Furthermore, the reactions were performed under biocompatible conditions, making this approach highly suitable for potential bioconjugation.

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Publication Details

Journal
Organic Letters
Published
2025-02-22
DOI
https://doi.org/10.1021/acs.orglett.5c00126
Citations
8
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
7.49

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article

Rapid C–S Coupling in Water via Ion-Pair-Catalyzed Dehydration

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8 citations
Organic Letters
Sulfur-Based Synthesis Techniques
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article

Rapid C–S Coupling in Water via Ion-Pair-Catalyzed Dehydration

Qianchi Lin, Zhenhua Jia, Teck‐Peng Loh, Chao Yang, Chen Peng, Yufei Zhu, Jinling Li
article en
8 citations

Abstract

The C-S bond is of significant importance due to its unique properties and diverse roles in chemistry, biology, and materials science. In this work, we present an efficient synthetic protocol of a rapidly dehydrative C-S coupling reaction with alcohols and thiols in water catalyzed by a triaryl-carbenium ion pair. Under metal-free conditions, a wide range of thioethers were obtained in good yields (up to 99%) with excellent functional group tolerance, including the fast modification of amino acid derivatives and functional molecules. This method allowed reactions to be conducted with low catalyst loading, down to 1.0 mol %, and was practical for gram-scale synthesis. Furthermore, the reactions were performed under biocompatible conditions, making this approach highly suitable for potential bioconjugation.

Organic LettersVol. 27(9)
Nanyang Technological University (SG), Henan University of Technology (CN), Division of Chemistry (US)
Agency for Science, Technology and Research, Ministry of Education - Singapore, Nanyang Technological University, National Natural Science Foundation of China, Henan University of Technology
Clean water and sanitation
Openalex Percentile: Top 3%
Sulfur-Based Synthesis Techniques
7.49
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