Herein, we report a simple and efficient synthetic approach for direct amidation of esters C(acyl)-O bond cleavage without any additional reagents or catalysts, using only water as a green solvent. Subsequently, the reaction byproduct is recovered and utilized for the next phase of ester synthesis. This method emphasized metal-free, additive-free, and base-free characteristics making it a new, sustainable, and eco-friendly way to realize direct amide bond formation. In addition, the synthesis of the drug molecule diethyltoluamide and the Gram-scale synthesis of a representative amide are demonstrated.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10186333 | PMC |
http://dx.doi.org/10.1039/d3ra02637j | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!