Bayesian Optimization of Solvent‐Free Thermal Amidation via Reactive Extrusion

A solvent-free thermo-mechanochemical synthesis of amides from carboxylic acids and amines, performed in an extruder, in the absence of coupling agents, additives, or catalyst is reported. A Bayesian optimization (BO) approach, incorporating an active and soft constraint, was developed, able to handle holistically various parameters (temperature, reaction time, excess of starting materials) while targeting a high conversion and sustainability. The methodology proved to be straightforward, high-yielding, sustainable, and easily adaptable to various substrates with a reduced number of experiments. It was applied to a variety of substrates, providing an easy and efficient preparation method of amides, including bioactive macamides and the active pharmaceutical ingredient (API) moclobemide. Optimized conditions facilitated the product isolation, some of them were obtained essentially pure from the extruder, others purified by extraction or crystallization. Notably, moclobemide could be synthesized at larger scale and isolated in the complete absence of organic solvent.

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Journal
Chemistry - A European Journal
Published
2026-03-26
DOI
https://doi.org/10.1002/chem.70914
Primary Topic
Chemical Synthesis and Analysis
Type
article
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article

Bayesian Optimization of Solvent‐Free Thermal Amidation via Reactive Extrusion

Xavier Bantreil, Frédéric Lamaty, Matthieu Lavayssiere
Chemistry - A European Journal
Chemical Synthesis and Analysis
article

Bayesian Optimization of Solvent‐Free Thermal Amidation via Reactive Extrusion

Xavier Bantreil, Frédéric Lamaty, Matthieu Lavayssiere
article en

Abstract

A solvent-free thermo-mechanochemical synthesis of amides from carboxylic acids and amines, performed in an extruder, in the absence of coupling agents, additives, or catalyst is reported. A Bayesian optimization (BO) approach, incorporating an active and soft constraint, was developed, able to handle holistically various parameters (temperature, reaction time, excess of starting materials) while targeting a high conversion and sustainability. The methodology proved to be straightforward, high-yielding, sustainable, and easily adaptable to various substrates with a reduced number of experiments. It was applied to a variety of substrates, providing an easy and efficient preparation method of amides, including bioactive macamides and the active pharmaceutical ingredient (API) moclobemide. Optimized conditions facilitated the product isolation, some of them were obtained essentially pure from the extruder, others purified by extraction or crystallization. Notably, moclobemide could be synthesized at larger scale and isolated in the complete absence of organic solvent.

Chemistry - A European Journal
École Nationale Supérieure de Chimie de Montpellier (FR), Centre National de la Recherche Scientifique (FR), Institut Universitaire de France (FR), Université de Montpellier (FR), Institut des Biomolécules Max Mousseron (FR)
Responsible consumption and production
Openalex Percentile: Top 6%
Chemical Synthesis and Analysis
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Bayesian Optimization of Solvent‐Free Thermal Amidation via Reactive Extrusion — Xavier Bantreil, Frédéric Lamaty, et al. · Chemistry - A European Journal (2026) | TGRS Research Map | TGRS