A Completely Metal‐Free Protocol for Oxidative Desulfitative C−N Coupling Reaction in Non‐Basic Condition

A metal free oxidative desulfitative C-N coupling reaction through activation of latent thiol group using hypervalent iodine reagent is being reported in eco-friendly solvent ethanol. Here, the thio-amide group present in 5-alkylidene-rhodanine has been utilized as latent thiol functionality and C-N coupling with amines is realized. The reaction occurs evading the use of metal catalysts, inert atmosphere, high temperature or microwave heating, and strong base which is normally required for metal catalyzed C-N coupling reaction. Pertinently, here poorly nucleophilic aromatic amines react very efficiently. Desulfitative C-N coupling involving free thiol moiety and poorly nucleophilic aromatic amines in metal free condition has never been accomplished in one step, without requiring high temperature microwave heating or strong bases. The reaction occurs at just 50 °C in few hours under ambient atmosphere. Moreover, here no H<sub>2</sub>S is released in the environment, since solid sulphur is precipitated out as side product, making this protocol environmentally friendly. Metal free condition, low temperature, use of non-toxic solvent and reagent, prevention of the release of H<sub>2</sub>S in the environment make this protocol very much environmentally friendly and highly suitable for C-N coupling in a sustainable way.

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Publication Details

Journal
Chemistry - An Asian Journal
Published
2025-03-11
DOI
https://doi.org/10.1002/asia.202401575
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

A Completely Metal‐Free Protocol for Oxidative Desulfitative C−N Coupling Reaction in Non‐Basic Condition

Subhajit Goswami, Partha Pratim Das, Souvik Mondal, Suman Ray et al.
Chemistry - An Asian Journal
Catalytic C–H Functionalization Methods
article

A Completely Metal‐Free Protocol for Oxidative Desulfitative C−N Coupling Reaction in Non‐Basic Condition

Subhajit Goswami, Partha Pratim Das, Souvik Mondal, Suman Ray, Aritra Mondal, Paramita Das
article en

Abstract

A metal free oxidative desulfitative C-N coupling reaction through activation of latent thiol group using hypervalent iodine reagent is being reported in eco-friendly solvent ethanol. Here, the thio-amide group present in 5-alkylidene-rhodanine has been utilized as latent thiol functionality and C-N coupling with amines is realized. The reaction occurs evading the use of metal catalysts, inert atmosphere, high temperature or microwave heating, and strong base which is normally required for metal catalyzed C-N coupling reaction. Pertinently, here poorly nucleophilic aromatic amines react very efficiently. Desulfitative C-N coupling involving free thiol moiety and poorly nucleophilic aromatic amines in metal free condition has never been accomplished in one step, without requiring high temperature microwave heating or strong bases. The reaction occurs at just 50 °C in few hours under ambient atmosphere. Moreover, here no H<sub>2</sub>S is released in the environment, since solid sulphur is precipitated out as side product, making this protocol environmentally friendly. Metal free condition, low temperature, use of non-toxic solvent and reagent, prevention of the release of H<sub>2</sub>S in the environment make this protocol very much environmentally friendly and highly suitable for C-N coupling in a sustainable way.

Chemistry - An Asian JournalVol. 20(7)
Presidency University (IN), Instituto Nacional de las Mujeres (MX)
Life in Land, Responsible consumption and production
Openalex Percentile: Top 97%
Catalytic C–H Functionalization Methods
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A Completely Metal‐Free Protocol for Oxidative Desulfitative C−N Coupling Reaction in Non‐Basic Condition — Subhajit Goswami, Partha Pratim Das, et al. · Chemistry - An Asian Journal (2025) | TGRS Research Map | TGRS