Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.
Angew Chem Int Ed Engl. 2016 Mar 7;55(11):3781-4. doi: 10.1002/anie.201511689. Epub 2016 Feb 16.
Mechanochemical conditions have been applied to an iridium(III)-catalyzed C-H bond amidation process for the first time. In the absence of solvent, the mechanochemical activation enables the formation of an iridium species that catalyzes the ortho-selective amidation of benzamides with sulfonyl azides as the nitrogen source. As the reaction proceeds in the absence of organic solvents without external heating and yields the desired products in excellent yields within short reaction times, this method constitutes a powerful, fast, and environmentally benign alternative to the common solvent-based standard approaches.
机械化学条件首次被应用于铱(III)催化的 C-H 键酰胺化过程。在没有溶剂的情况下,机械化学活化使得形成一种铱物种成为可能,该物种催化苯甲酰胺与磺酰叠氮作为氮源的邻选择性酰胺化。由于该反应在没有有机溶剂、无需外部加热的情况下进行,并且在短时间内以优异的收率得到所需产物,因此该方法是对常见的基于溶剂的标准方法的一种强大、快速和环境友好的替代方法。