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Updated: May 19, 2026

Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
Efficient and selective multicomponent oxidative coupling of two different aliphatic primary amines into thioamides
Thanh Binh Nguyen1, Ludmila Ermolenko, Ali Al-Mourabit
1Centre de Recherche de Gif-sur-Yvette, Institut de Chimie des Substances Naturelles CNRS, 91198 Gif-sur-Yvette Cedex, France. nguyen@icsn.cnrs-gif.fr
Researchers developed a new method for synthesizing thioamides from amines and sulfur. This efficient, solvent-free process offers a selective route to valuable chemical compounds.
Area of Science:
- Organic Chemistry
- Synthetic Chemistry
Background:
- Thioamides are important functional groups in medicinal chemistry and materials science.
- Existing synthetic methods often require harsh conditions or multiple steps.
Purpose of the Study:
- To develop an efficient and selective method for synthesizing thioamides.
- To utilize readily available starting materials and minimize waste.
Main Methods:
- A multicomponent oxidative coupling reaction was employed.
- Elemental sulfur was used as the sulfur source.
- The reaction was performed under solvent-free conditions.
Main Results:
- Two different aliphatic primary amines were successfully coupled.
- High yields of the desired thioamides were obtained.
- The reaction demonstrated good selectivity.
Conclusions:
- A novel, efficient, and selective synthesis of thioamides has been established.
- The developed method offers a sustainable and practical approach for thioamide preparation.
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