Chinese Journal of Organic Chemistry ›› 2026, Vol. 46 ›› Issue (8): 3147-3157.DOI: 10.6023/cjoc202602012 Previous Articles     Next Articles

ARTICLES

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)

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