Mart Mehmet, Jurczak Janusz, Karakaya Idris
Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka, 44/52, 01-224, Warsaw, Poland.
Department of Chemistry, College of Basic Sciences, Gebze Technical University, 41400 Gebze, Turkey.
Org Biomol Chem. 2022 Oct 19;20(40):7900-7906. doi: 10.1039/d2ob01322c.
A novel and efficient catalyst- and activating agent-free amidation method direct amidation of carboxylic acids where carbodiimides act as a reagent instead of an activating agent is reported. The reaction is conducted under non-traditional coupling conditions where a higher temperature is employed. Besides not using stoichiometric ratios of activating agent or catalyst, this approach is made even more attractive by occurring in the presence of the environmentally friendly and recyclable non-toxic solvent of DMSO. A wide variety of benzylic, aliphatic, α,β-unsaturated and aromatic carboxylic acids provide related amides in up to 95% yield. The excellent yield from a gram-scale reaction shows that this application is particularly convenient for larger-scale synthesis applications.
报道了一种新颖、高效的无催化剂和活化剂的酰胺化方法,即羧酸的直接酰胺化反应,其中碳二亚胺作为试剂而非活化剂。该反应在采用较高温度的非传统偶联条件下进行。除了不使用化学计量比的活化剂或催化剂外,该方法在环境友好且可回收的无毒二甲基亚砜溶剂存在下进行,这使其更具吸引力。多种苄基、脂肪族、α,β-不饱和和芳香族羧酸能以高达95%的产率提供相应的酰胺。克级反应的优异产率表明,该应用对于大规模合成应用特别方便。