Multicomponent Reaction for the Synthesis of β-Ketosulfides in Deep Eutectic Solvents

The use of Type III Deep Eutectic Solvents (DESs) as both solvents and cocatalysts enable the one-pot synthesis of several β-ketosulfides, structural motifs commonly found in biologically active compounds, via a multicomponent reaction (MCR) involving 2-bromoketones, alkyl or benzyl halides, and potassium thioacetate in basic medium. Under these conditions, it was possible to avoid not only the use of the non-eco-friendly solvent dimethylformamide (DMF), but also an additional hydrolytic step previously reported for the preparation of these molecules. The MCR conducted in the presence of the DES ChCl:Gly (1:2) was optimized through the evaluation of different reaction parameters. Notably, the non-conventional medium could be recycled up to four times without any appreciable loss of catalytic activity. Environmental metrics, including the E factor, E+ factor, and Global Warming Potential (GWP), were calculated for the process both in the presence and absence of the DES, demonstrating improved environmental performance when the DES was employed.

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Journal
Molecules
Published
2026-02-22
DOI
https://doi.org/10.3390/molecules31040745
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

Multicomponent Reaction for the Synthesis of β-Ketosulfides in Deep Eutectic Solvents

Andrés R. Alcántara, Chiara Falcini, Rosario Fernández, Gonzalo de Gonzalo et al.
Molecules
Sulfur-Based Synthesis Techniques
article

Multicomponent Reaction for the Synthesis of β-Ketosulfides in Deep Eutectic Solvents

Andrés R. Alcántara, Chiara Falcini, Rosario Fernández, Gonzalo de Gonzalo, David Jaén-Herrera
article en

Abstract

The use of Type III Deep Eutectic Solvents (DESs) as both solvents and cocatalysts enable the one-pot synthesis of several β-ketosulfides, structural motifs commonly found in biologically active compounds, via a multicomponent reaction (MCR) involving 2-bromoketones, alkyl or benzyl halides, and potassium thioacetate in basic medium. Under these conditions, it was possible to avoid not only the use of the non-eco-friendly solvent dimethylformamide (DMF), but also an additional hydrolytic step previously reported for the preparation of these molecules. The MCR conducted in the presence of the DES ChCl:Gly (1:2) was optimized through the evaluation of different reaction parameters. Notably, the non-conventional medium could be recycled up to four times without any appreciable loss of catalytic activity. Environmental metrics, including the E factor, E+ factor, and Global Warming Potential (GWP), were calculated for the process both in the presence and absence of the DES, demonstrating improved environmental performance when the DES was employed.

MoleculesVol. 31(4)
Universidad Complutense de Madrid (ES), Universidad de Sevilla (ES)
Openalex Percentile: Top 46%
Sulfur-Based Synthesis Techniques
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Multicomponent Reaction for the Synthesis of β-Ketosulfides in Deep Eutectic Solvents — Andrés R. Alcántara, Chiara Falcini, et al. · Molecules (2026) | TGRS Research Map | TGRS