Functionalization of Electron-Rich Secondary Benzyl Alcohols in HFIP: From Thioethers to Trisubstituted Methanes

To date, C-S bond formation via dehydration of electron-rich secondary benzylic alcohols has been limited to catalytic approaches. In this work, we developed an efficient method for synthesizing various thioethers by employing hexafluoroisopropanol (HFIP) as a solvent. This approach also enables the functionalization of secondary benzyl alcohols with other important organic molecules, such as allylsilanes, activated arenes, and indoles, leading to various trisubstituted methanes, including 14 novel products in total.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-06-28
DOI
https://doi.org/10.1021/acs.joc.5c00900
Citations
5
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
4.68

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article

Functionalization of Electron-Rich Secondary Benzyl Alcohols in HFIP: From Thioethers to Trisubstituted Methanes

Krzysztof Kuciński, Martyna Markwitz, Klaudiusz Labrzycki, Kacper Łyczek
5 citations
The Journal of Organic Chemistry
Sulfur-Based Synthesis Techniques
4.68
article

Functionalization of Electron-Rich Secondary Benzyl Alcohols in HFIP: From Thioethers to Trisubstituted Methanes

Krzysztof Kuciński, Martyna Markwitz, Klaudiusz Labrzycki, Kacper Łyczek
article en
5 citations

Abstract

To date, C-S bond formation via dehydration of electron-rich secondary benzylic alcohols has been limited to catalytic approaches. In this work, we developed an efficient method for synthesizing various thioethers by employing hexafluoroisopropanol (HFIP) as a solvent. This approach also enables the functionalization of secondary benzyl alcohols with other important organic molecules, such as allylsilanes, activated arenes, and indoles, leading to various trisubstituted methanes, including 14 novel products in total.

The Journal of Organic ChemistryVol. 90(27)
Adam Mickiewicz University in Poznań (PL)
Narodowe Centrum Nauki
Openalex Percentile: Top 5%
Sulfur-Based Synthesis Techniques
4.68
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