Ebrahimzadeh Farzaneh
Department of Chemistry, Marvdasht Branch, Islamic Azad University, Marvdasht, Iran.
Turk J Chem. 2024 Oct 14;49(2):133-142. doi: 10.55730/1300-0527.3717. eCollection 2025.
The in situ generation of the Vilsmeier-Haack complex was studied by combining FeO@SiO@CS@POCl with ,dimethylformamide (DMF), demonstrating remarkable efficiency and regioselectivity in transforming epoxides into β-bromoformates. The reported yields were notably high and were achieved under mild reaction conditions. Interestingly, the removal of DMF led to the synthesis of -dihalide compounds. The product of this transformation depended on the specific details of how the experiment was done, highlighting how sensitive the process is to different ways of conducting the experiment. The use of a magnetic core-shell catalyst, FeO@SiO@CS@POCl, facilitates a straightforward work-up procedure, simplifying the isolation of the desired products. Furthermore, the reactions were conducted under clean and neutral conditions, contributing to their environmentally friendly nature.
通过将FeO@SiO@CS@POCl与二甲基甲酰胺(DMF)结合,研究了原位生成Vilsmeier - Haack配合物的过程,结果表明在将环氧化物转化为β - 溴甲酸酯方面具有显著的效率和区域选择性。报道的产率非常高,且是在温和的反应条件下实现的。有趣的是,去除DMF会导致合成二卤化物化合物。这种转化的产物取决于实验进行的具体细节,突出了该过程对不同实验操作方式的敏感性。使用磁性核壳催化剂FeO@SiO@CS@POCl有助于简化后处理程序,简化了所需产物的分离。此外,反应是在清洁和中性条件下进行的,这有助于其环境友好的特性。