Highly efficient AgNO<sub>3</sub>
-catalyzed approach to 2-(benzo[<i>d</i>
]azol-2-yl)phenols from salicylaldehydes with 2-aminothiophenol, 2-aminophenol and benzene-1,2-diamine
derivatives in good to excellent yields (63–98%) is described. The reaction proceeds via condensation/intramolecular nucleophilic addition/oxidation process between substituted salicylaldehydes and 2‐aminothiophenol, 2‐aminophenol or benzene‐1,2‐diamine under mild reaction conditions. Notably, this reaction utilizes cheap AgNO3 as a readily available and low‐cost benign oxidant at low catalyst loadings with
描述了一种新的,便捷有效的AgNO 3催化策略,用于制备2-(苯并[ d ] azol-2-基)苯酚衍生物,产率高至优异(63-98%)。反应在温和的反应条件下通过取代的水杨醛与2-氨基硫酚,2-氨基酚或苯1,2-二胺之间的缩合/分子内亲核加成/氧化过程进行。值得注意的是,该反应利用廉价的AgNO 3作为易于获得的低成本良性氧化剂,催化剂负载低,具有出色的官能团耐受性。
Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives
A novel, one-pot, phenylboronic acid catalyzed, cyanide promoted synthesis of 2-(2-hydroxyphenyl)benzoxazoles from salicylaldehydes and o-aminophenols is described. The synthesis is characterized by mild conditions, short reaction times, and simple workup of crystalline, high purity products. (C) 2011 Elsevier Ltd. All rights reserved.