# From perfluoroalkyl aryl sulfoxides to ortho thioethers

**Authors:** Yang Li, Guillaume Dagousset, Emmanuel Magnier, Bruce Pégot

PMC · DOI: 10.3762/bjoc.20.181 · Beilstein Journal of Organic Chemistry · 2024-08-23

## TL;DR

A new method was developed to create ortho thioether derivatives using a [3,3]-rearrangement from perfluoroalkyl aryl sulfoxides.

## Contribution

The paper introduces a one-pot two-step protocol for synthesizing original ortho thioether derivatives.

## Key findings

- A [3,3]-rearrangement enabled the synthesis of aryl-SCF3 compounds.
- Variation of nitriles and trifluoroalkyl sulfoxides produced diverse aryl-SCF3 derivatives.
- Modifications to the perfluoroalkyl chain were successfully achieved.

## Abstract

Access to original ortho thioether derivatives was achieved through a [3,3]-rearrangement in a one-pot two-step protocol. Several aryl-SCF3 compounds are reported by variation of the nitrile or of the trifluoroalkyl sulfoxide starting material. The variation of the perfluoroalkyl chain was also possible.

## Linked entities

- **Chemicals:** SCF3 (PubChem CID 83678)

## Full-text entities

- **Chemicals:** aryl-SCF3 (-), nitrile (MESH:D009570), thioether (MESH:D013440)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11346307/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11346307/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC11346307/full.md

---
Source: https://tomesphere.com/paper/PMC11346307