A Remarkably Simple Aza-Michael Reaction with Citrus Fruit Juice

Introduction: Citrus fruit juice is used in the Aza-Michael reaction of secondary amines with carbonyl compounds. Clearly, citrus fruit juice acts as a solvent and an acidic catalyst. More-over, the reaction proceeds well at room temperature and produces the products in high yields. The Aza-Michael addition is a widely used carbon–nitrogen bond-forming reaction in organic syn-thesis, traditionally requiring catalysts, organic solvents, or elevated temperatures. With increasing focus on green chemistry, there is a demand for sustainable reaction conditions that are both effec-tive and environmentally benign. This study explores a novel approach using common citrus fruit juice as a natural, eco-friendly medium for promoting the Aza-Michael reaction. Methods: Fresh citrus juices (lemon, lime, and orange) were extracted and used without modifica-tion. A series of amines were reacted with α,β-unsaturated carbonyl compounds in the juice medium at room temperature. Reactions were monitored by thin-layer chromatography (TLC). Products were isolated via standard extraction and characterized using NMR. Results: Efficient Aza-Michael addition reactions were achieved using citrus juices, especially lemon juice, due to its high citric acid content and low pH. The reactions proceeded at room tem-perature, without any added catalyst or organic solvent. A variety of amines and Michael acceptors yielded the corresponding adducts in good to excellent yields. The method displayed good func-tional group tolerance and reproducibility. Discussion: The Michael reaction of secondary amines with unsaturated ketones and esters in citrus juice yields high products. Lime juice reacts faster due to its high acidity, allowing for easy opera-tion, environmentally friendly reaction conditions, green chemistry, fast reactions, and high product yields. Conclusion: This study introduces an innovative and practical green chemistry approach to a classic organic reaction. The use of citrus juice as a natural reaction medium offers a safe, cost-effective, and biodegradable alternative to conventional synthetic protocols.

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Publication Details

Journal
Current Organocatalysis
Published
2026-01-07
DOI
https://doi.org/10.2174/0122133372406529251103075202
Primary Topic
Multicomponent Synthesis of Heterocycles
Type
article
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article

A Remarkably Simple Aza-Michael Reaction with Citrus Fruit Juice

Dilip K. Maiti, Ram Naresh Yadav, Bimal Krishna Banik, Antara Roy
Current Organocatalysis
Multicomponent Synthesis of Heterocycles
article

A Remarkably Simple Aza-Michael Reaction with Citrus Fruit Juice

Dilip K. Maiti, Ram Naresh Yadav, Bimal Krishna Banik, Antara Roy
article en

Abstract

Introduction: Citrus fruit juice is used in the Aza-Michael reaction of secondary amines with carbonyl compounds. Clearly, citrus fruit juice acts as a solvent and an acidic catalyst. More-over, the reaction proceeds well at room temperature and produces the products in high yields. The Aza-Michael addition is a widely used carbon–nitrogen bond-forming reaction in organic syn-thesis, traditionally requiring catalysts, organic solvents, or elevated temperatures. With increasing focus on green chemistry, there is a demand for sustainable reaction conditions that are both effec-tive and environmentally benign. This study explores a novel approach using common citrus fruit juice as a natural, eco-friendly medium for promoting the Aza-Michael reaction. Methods: Fresh citrus juices (lemon, lime, and orange) were extracted and used without modifica-tion. A series of amines were reacted with α,β-unsaturated carbonyl compounds in the juice medium at room temperature. Reactions were monitored by thin-layer chromatography (TLC). Products were isolated via standard extraction and characterized using NMR. Results: Efficient Aza-Michael addition reactions were achieved using citrus juices, especially lemon juice, due to its high citric acid content and low pH. The reactions proceeded at room tem-perature, without any added catalyst or organic solvent. A variety of amines and Michael acceptors yielded the corresponding adducts in good to excellent yields. The method displayed good func-tional group tolerance and reproducibility. Discussion: The Michael reaction of secondary amines with unsaturated ketones and esters in citrus juice yields high products. Lime juice reacts faster due to its high acidity, allowing for easy opera-tion, environmentally friendly reaction conditions, green chemistry, fast reactions, and high product yields. Conclusion: This study introduces an innovative and practical green chemistry approach to a classic organic reaction. The use of citrus juice as a natural reaction medium offers a safe, cost-effective, and biodegradable alternative to conventional synthetic protocols.

Current OrganocatalysisVol. 13
University of Calcutta (IN), Prince Mohammad bin Fahd University (SA), Veer Bahadur Singh Purvanchal University (IN)
Responsible consumption and production
Openalex Percentile: Top 94%
Multicomponent Synthesis of Heterocycles
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