A unified flow strategy for the preparation and use of trifluoromethyl-heteroatom anions

The trifluoromethyl group (CF<sub>3</sub>) is a key functionality in pharmaceutical and agrochemical development, greatly enhancing the efficacy and properties of resulting compounds. However, attaching the CF<sub>3</sub> group to heteroatoms such as sulfur, oxygen, and nitrogen poses challenges because of the lack of general synthetic methods and reliance on bespoke reagents. Here, we present a modular flow platform that streamlines the synthesis of heteroatom-CF<sub>3</sub> motifs. Our method uses readily available organic precursors in combination with cesium fluoride as the primary fluorine source, facilitating the rapid generation of <i>N</i>-trifluoromethyl(R) [NCF<sub>3</sub>(R)], SCF<sub>3</sub> (trifluoromethylthio), and OCF<sub>3</sub> (trifluoromethoxy) anions on demand without reliance on perfluoroalkyl precursor reagents. This strategy offers a more environmentally friendly synthesis of trifluoromethyl(heteroatom)-containing molecules, with the potential for scalability in manufacturing processes facilitated by flow technology.

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Publication Details

Journal
Science
Published
2024-08-29
DOI
https://doi.org/10.1126/science.adq2954
Citations
37
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
7.70

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article

A unified flow strategy for the preparation and use of trifluoromethyl-heteroatom anions

Mauro Spennacchio, James J. Douglas, Omar Boutureira, Marco Colella et al.
37 citations
Science
Fluorine in Organic Chemistry
7.70
article

A unified flow strategy for the preparation and use of trifluoromethyl-heteroatom anions

Mauro Spennacchio, James J. Douglas, Omar Boutureira, Marco Colella, Daniele Mazzarella, Timothy Noël, Jelena Stanić, Miguel Bernús
article en
37 citations

Abstract

The trifluoromethyl group (CF<sub>3</sub>) is a key functionality in pharmaceutical and agrochemical development, greatly enhancing the efficacy and properties of resulting compounds. However, attaching the CF<sub>3</sub> group to heteroatoms such as sulfur, oxygen, and nitrogen poses challenges because of the lack of general synthetic methods and reliance on bespoke reagents. Here, we present a modular flow platform that streamlines the synthesis of heteroatom-CF<sub>3</sub> motifs. Our method uses readily available organic precursors in combination with cesium fluoride as the primary fluorine source, facilitating the rapid generation of <i>N</i>-trifluoromethyl(R) [NCF<sub>3</sub>(R)], SCF<sub>3</sub> (trifluoromethylthio), and OCF<sub>3</sub> (trifluoromethoxy) anions on demand without reliance on perfluoroalkyl precursor reagents. This strategy offers a more environmentally friendly synthesis of trifluoromethyl(heteroatom)-containing molecules, with the potential for scalability in manufacturing processes facilitated by flow technology.

ScienceVol. 385(6712)
University of Padua (IT), AstraZeneca (Singapore) (SG), University of Bari Aldo Moro (IT), Universitat Rovira i Virgili (ES), University of Amsterdam (NL)
European Commission, Horizon 2020 Framework Programme, European Regional Development Fund, Agencia Estatal de Investigación
Responsible consumption and production
Openalex Percentile: Top 2%
Fluorine in Organic Chemistry
7.70
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