Kondo Keisuke, Kubota Koji, Ito Hajime
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University Sapporo Hokkaido Japan
Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University Sapporo Hokkaido Japan.
Chem Sci. 2024 Feb 12;15(12):4452-4457. doi: 10.1039/d3sc06052g. eCollection 2024 Mar 20.
In this study, a mechanochemical protocol for highly efficient and ammonia-free sodium-based Birch reduction was developed, leveraging the use of cheap and easy-to-handle sodium lumps. The key to achieving this transformation is the use of d-(+)-glucose as a proton source, which solidifies the reaction mixture in bulk state, enhancing the efficiency of the mechanical activation of sodium lumps through the ball-milling process. Under the developed conditions, a diverse array of aromatic and heteroaromatic compounds were selectively reduced to produce the corresponding 1,4-cyclohexadiene derivatives in high yields within 30 min. Notably, all synthetic operations can be carried out without inert gases or the need for dry or bulk organic solvents. Furthermore, a scaled-up synthesis can be conducted without any yield losses. These results suggest that the present mechanochemical approach offers a more convenient, economically attractive, and sustainable alternative to previously established Birch reduction protocols.
在本研究中,开发了一种用于高效无氨钠基伯奇还原反应的机械化学方法,该方法利用了廉价且易于处理的钠块。实现这种转化的关键是使用d-(+)-葡萄糖作为质子源,它能使反应混合物整体固化,通过球磨过程提高钠块机械活化的效率。在优化条件下,多种芳香族和杂芳香族化合物被选择性还原,在30分钟内高产率地生成相应的1,4-环己二烯衍生物。值得注意的是,所有合成操作均可在无惰性气体的条件下进行,且无需干燥或大量有机溶剂。此外,放大合成时不会有产率损失。这些结果表明,当前的机械化学方法为先前已确立的伯奇还原反应方法提供了一种更便捷、经济上更具吸引力且可持续的替代方案。