Yu Haifeng, Zhang Zheyu, Zhang Xue, Xu Yupeng, Huo Dongyue, Zhang Lanyun, Wang Wenju
College of Chemistry, Baicheng Normal University, Baicheng, Jilin 137000, China.
J Org Chem. 2022 Mar 4;87(5):2985-2996. doi: 10.1021/acs.joc.1c02825. Epub 2022 Feb 8.
For the first time, an eco-friendly and sustainable tandem [5C + 1C] cycloaromatization of α-alkenoyl ketene dithioacetals and nitroethane in water for the efficient synthesis of -acylphenols was reported. In refluxing water, a range of α-alkenoyl ketene dithioacetals and nitroethane smoothly underwent tandem Michael addition/cyclization/aromatization reactions in the presence of 2.0 equivalents of DBU to provide various -acylphenols in excellent yields. The green approach to -acylphenols not only avoided the use of harmful organic solvents, which could result in serious environmental and safety issues, but also exhibited fascinating features such as good substrate scope, excellent yields, simple purification for desired products, ease of scale-up, and reusable aqueous medium.
首次报道了在水中进行α-烯丙酰基乙烯酮二硫代缩醛与硝基乙烷的环保且可持续的串联[5C + 1C]环芳构化反应,用于高效合成α-酰基酚。在回流的水中,一系列α-烯丙酰基乙烯酮二硫代缩醛和硝基乙烷在2.0当量的DBU存在下顺利进行串联迈克尔加成/环化/芳构化反应,以优异的产率提供各种α-酰基酚。这种合成α-酰基酚的绿色方法不仅避免了使用可能导致严重环境和安全问题的有害有机溶剂,而且还具有底物范围广、产率优异、目标产物纯化简单、易于放大以及水相介质可重复使用等吸引人的特点。