A transition-metal-free synthetic method has been developed for the synthesis of unsymmetrical diaryl chalcogenides (S, Se, and Te) from diaryl dichalcogenides and arenes under oxidative conditions by using potassium persulfate at room temperature. Variously substituted arenes such as anisole, thioanisole, diphenyl ether, phenol, naphthol, di- and trimethoxy benzenes, xylene, mesitylene, N,N-dimethylaniline
已开发出一种无过渡金属的合成方法,该方法用于在室温条件下通过使用过硫酸钾,在氧化条件下由二芳基二卤化锑和芳烃合成不对称的二芳基硫属元素化物(S,Se和Te)。各种取代的芳烃,例如苯甲醚,硫代苯甲醚,二苯醚,苯酚,萘酚,二和三甲氧基苯,二甲苯,均三甲苯,N,N-二甲基苯胺,溴取代的芳烃,萘和二芳基二卤化碳经历了碳硫族键形成反应在三氟乙酸中生成不对称的二芳基硫属元素化物。为了理解反应的机理部分,由77进行了详细的中间体原位表征通过使用二苯基二硒化物为底物进行Se NMR光谱分析。77 Se NMR研究表明,亲电子物质ArE +是由二芳基二卤化二硫化物与过硫酸盐在三氟乙酸中反应生成的。芳基硫属元素离子对芳烃的亲电攻击可能是芳基-硫属元素键形成的原因。
Iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature
作者:Hua Tian、Changjin Zhu、Haijun Yang、Hua Fu
DOI:10.1039/c4cc03600j
日期:——
A simple, efficient and environmentally friendly method for iron or boron-catalyzed C–H arylthiation of substituted phenols at room temperature has been developed, and the corresponding diaryl sulfides were prepared in good to excellent yields.