有机化学 ›› 2026, Vol. 46 ›› Issue (8): 3147-3157.DOI: 10.6023/cjoc202602012 上一篇    下一篇

研究论文

酰胺噁唑啉导向的铜催化[2.2]对环芳烷直接C—H酰氧基化反应

韩银松, 王东炜, 肖佳怡, 冯若昆*()   

  1. 绍兴大学化学化工学院 浙江绍兴 312000
  • 收稿日期:2026-02-10 修回日期:2026-04-05 发布日期:2026-05-18
  • 通讯作者: 冯若昆
  • 基金资助:
    浙江省自然科学基金(LQ15B020002); 绍兴市重点科技创新团队(202034); 国家级大学生创新创业训练计划(202410349028)

Amide-Oxazoline-Directed Copper-Catalyzed C—H Acyloxylation of [2.2]Paracyclophanes

Yinsong Han, Dongwei Wang, Jiayi Xiao, Ruokun Feng*()   

  1. College of Chemistry and Chemical Engineering, Shaoxing University, Shaoxing, Zhejiang 312000
  • Received:2026-02-10 Revised:2026-04-05 Published:2026-05-18
  • Contact: Ruokun Feng
  • Supported by:
    Zhejiang Provincial Natural Science Foundation(LQ15B020002); Shaoxing Key Science and Technology Innovation Team Project(202034); National College Students’ Innovation and Entrepreneurship Training Program(202410349028)

报道了一种基于廉价金属铜催化、利用酰胺噁唑啉导向基团实现的[2.2]对环芳烷直接C(sp2)—H酰氧化反应. 该反应体系适用于芳香羧酸、烯基羧酸及烷基羧酸等多种羧酸底物, 能以中等到良好的产率获得目标产物. 克级规模实验及后续水解反应进一步证明了该方法的合成实用性. 本研究为[2.2]对环芳烷的选择性官能化提供了一种高效、便捷的合成策略, 具有潜在的应用前景.

关键词: 铜催化, 酰胺噁唑啉导向, C—H酰氧基化, [2.2]对环芳烷

A copper-catalyzed direct C—H acyloxylation of [2.2]paracyclophanes utilizing an oxazoline amide directing group has been developed. A range of carboxylic acid substrates, including aromatic, alkenyl, and alkyl carboxylic acids, are tolerated, delivering the corresponding acyloxylated products in moderate to good yields. Gram-scale reactions and subsequent hydrolysis experiments further demonstrate the synthetic utility of this method. This work provides an efficient and convenient strategy for the selective functionalization of [2.2]paracyclophanes, highlighting its potential for practical applications.

Key words: copper catalysis, amide oxazoline directing, C—H acyloxylation, [2.2]paracyclophanes