Takahashi Rina, Hu Anqi, Gao Pan, Gao Yunpeng, Pang Yadong, Seo Tamae, Jiang Julong, Maeda Satoshi, Takaya Hikaru, Kubota Koji, Ito Hajime
Division of Applied Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Nat Commun. 2021 Nov 18;12(1):6691. doi: 10.1038/s41467-021-26962-w.
Since the discovery of Grignard reagents in 1900, the nucleophilic addition of magnesium-based carbon nucleophiles to various electrophiles has become one of the most powerful, versatile, and well-established methods for the formation of carbon-carbon bonds in organic synthesis. Grignard reagents are typically prepared via reactions between organic halides and magnesium metal in a solvent. However, this method usually requires the use of dry organic solvents, long reaction times, strict control of the reaction temperature, and inert-gas-line techniques. Despite the utility of Grignard reagents, these requirements still represent major drawbacks from both an environmental and an economic perspective, and often cause reproducibility problems. Here, we report the general mechanochemical synthesis of magnesium-based carbon nucleophiles (Grignard reagents in paste form) in air using a ball milling technique. These nucleophiles can be used directly for one-pot nucleophilic addition reactions with various electrophiles and nickel-catalyzed cross-coupling reactions under solvent-free conditions.
自1900年发现格氏试剂以来,基于镁的碳亲核试剂与各种亲电试剂的亲核加成反应已成为有机合成中形成碳-碳键最强大、用途最广泛且最成熟的方法之一。格氏试剂通常通过有机卤化物与镁金属在溶剂中反应制备。然而,这种方法通常需要使用干燥的有机溶剂、较长的反应时间、严格控制反应温度以及惰性气体管路技术。尽管格氏试剂很有用,但从环境和经济角度来看,这些要求仍然是主要缺点,并且常常导致重现性问题。在此,我们报道了使用球磨技术在空气中以机械化学方法通用合成基于镁的碳亲核试剂(膏状格氏试剂)。这些亲核试剂可直接用于在无溶剂条件下与各种亲电试剂进行的一锅法亲核加成反应以及镍催化的交叉偶联反应。