Nie Jinli, He Ziqing, Xie Sijie, Li Yibiao, He Runfa, Chen Lu, Luo Xiai
Jiangmen Key Laboratory of Synthetic Chemistry and Cleaner Production, School of Environmental & Chemical Engineering, Wuyi University, Jiangmen 529020, China.
Hunan Province Key Laboratory for Synthetic Biology of Traditional Chinese Medicine, School of Pharmaceutical Sciences, Hunan University of Medicine, Huaihua 418000, China.
Molecules. 2024 May 24;29(11):2485. doi: 10.3390/molecules29112485.
Thioethers are critical in the fields of pharmaceuticals and organic synthesis, but most of the methods for synthesis alkyl thioethers employ foul-smelling thiols as starting materials or generate them as by-products. Additionally, most thiols are air-sensitive and are easily oxidized to produce disulfides under atmospheric conditions; thus, a novel method for synthesizing thioethers is necessary. This paper reports a simple, effective, green method for synthesizing dialkyl or alkyl aryl thioether derivatives using odorless, stable, low-cost ROCSK as a thiol surrogate. This transformation offers a broad substrate scope and good functional group tolerance with excellent selectivity. The reaction likely proceeds via xanthate intermediates, which can be readily generated via the nucleophilic substitution of alkyl halides or aryl halides with ROCSK under transition-metal-free and base-free conditions.
硫醚在制药和有机合成领域至关重要,但大多数合成烷基硫醚的方法都使用有恶臭的硫醇作为起始原料或生成硫醇作为副产物。此外,大多数硫醇对空气敏感,在大气条件下很容易被氧化生成二硫化物;因此,需要一种合成硫醚的新方法。本文报道了一种简单、有效、绿色的方法,使用无味、稳定、低成本的ROCSK作为硫醇替代物来合成二烷基或烷基芳基硫醚衍生物。这种转化具有广泛的底物范围和良好的官能团耐受性,选择性优异。该反应可能通过黄原酸酯中间体进行,在无过渡金属和无碱条件下,卤代烃或芳基卤化物与ROCSK发生亲核取代反应可轻松生成黄原酸酯中间体。