Moghaddam Firouz Matloubi, Tavakoli Ghazal, Saeednia Borna, Langer Peter, Jafari Behzad
Laboratory of Organic Synthesis and Natural Products, Department of Chemistry, Sharif University of Technology , Azadi Street, 111559516 Tehran, Iran.
Institut für Chemie, Universität Rostock , Albert-Einstein-Strasse 3a, 18059 Rostock, Germany.
J Org Chem. 2016 May 6;81(9):3868-76. doi: 10.1021/acs.joc.6b00329. Epub 2016 Apr 21.
This study describes an efficient method for ortho-selective halogenation of N-arylcarbamates under mild conditions for the first time. Although being weakly coordinating, N-arylcarbamates act very well as a removable directing group for activation of C-H bonds. The developed procedure results in extremely valuable halogenated N-arylcarbmates that can further be hydrolyzed to halogenated anilines. The obtained reaction conditions showed broad scope and wide functional group tolerance. All the products were formed in good yields with extremely high selectivity.
本研究首次描述了一种在温和条件下对N-芳基氨基甲酸酯进行邻位选择性卤化的有效方法。尽管N-芳基氨基甲酸酯的配位能力较弱,但作为一种可去除的导向基团,它在活化C-H键方面表现出色。所开发的方法可得到极具价值的卤代N-芳基氨基甲酸酯,其可进一步水解为卤代苯胺。所获得的反应条件具有广泛的适用范围和良好的官能团耐受性。所有产物均以良好的产率和极高的选择性生成。