- Nanthini Rajendran Vellore Institute of Technology University ,
- Kiruthigadevi Kamaraj Vellore Institute of Technology University ,
- Saranya Janakiraman Vellore Institute of Technology University ,
- Mary Saral A Vellore Institute of Technology University ,
- Pierre. H. Dixneuf University of Rennes 1 ,
- Charles Beromeo Bheeter Vellore Institute of Technology University
Amides contain the paramount functional group in the field of chemistry as well as biology and they play a unique role in pharmaceutical industries. Amide bond formation is a prevalent reaction using coupling reagents, usually metal catalysts and additives etc. In this context, herein, we developed a simple and efficient synthetic approach for the direct amidation through esters, simply in water, affording the desired products in good to excellent yields. Interestingly, this method features metal-free, additive-free, and base-free characteristics, and it also uses water as a green solvent. Therefore, it is a new and eco-friendly way to realize the direct amide bond formation. Applying this methodology, we prepared over 30 different amides including the drug molecule Diethyltoluamide in good yield. Finally, this approach was successfully applied to the gram-scale synthesis of a representative amide product.
We have done more substrate scopes, including aromatic amines. Also, we included HPTLC measurements of our crude reaction to analyze the phenol.
A sustainable approach to amide bond formation via C-O bond cleavage of simple esters in water