大学化学 >> 2026, Vol. 41 >> Issue (5): 190-197.doi: 10.12461/PKU.DXHX202511104

所属专题: 第5届全国大学生化学实验创新设计大赛

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串联SNAr/Aldol缩合构建季碳稠合吲哚啉

贾丰成, 郑子侠, 李菲, 段辉琴, 王刚   

  1. 武汉工程大学化学与环境工程学院, 湖北 武汉 430205
  • 收稿日期:2025-11-17 录用日期:2026-02-26 发布日期:2026-05-21
  • 通讯作者: 贾丰成 E-mail:fengcheng-jia@wit.edu.cn Fengcheng Jia
  • 基金资助:
    武汉工程大学教学研究项目(X2023016)

Tandem SNAr/Aldol condensation for the constructruction of quaternary carbon-containing fused indoline

Fengcheng Jia, Zixia Zheng, Fei Li, Huiqin Duan, Gang Wang   

  1. School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430205, Hubei Province, China
  • Received:2025-11-17 Accepted:2026-02-26 Published:2026-05-21
  • Contact: Fengcheng Jia E-mail:fengcheng-jia@wit.edu.cn

摘要: 目前大学本科基础有机化学实验多为简单的单元反应,一锅法串联反应的实验项目较少。本实验以廉价易得的3-甲基-2-吲哚酮和2-氯-5-硝基苯乙酮为原料,设计了一个包含芳香亲核取代与Aldol缩合的串联反应,可以合成含季碳中心的2,3-稠合吲哚啉。本实验蕴含丰富的理论知识,具有操作简单、反应稳定和可重复性高等特点。

关键词: 串联环化反应, SNAr反应, Aldol缩合, 季碳稠合吲哚啉

Abstract: Current undergraduate organic chemistry experiments predominantly focus on simple single-step reactions, with limited exposure to one-pot tandem reactions. This experiment employs cost-effective and readily available starting materials, 3-methyl-2-indolinone and 2-chloro-5-nitroacetophenone, to demonstrate a tandem process combining aromatic nucleophilic substitution (SNAr) with Aldol condensation. The methodology enables the synthesis of 2,3-fused indoline derivatives featuring a quaternary carbon center. The experiment incorporates substantial theoretical concepts while maintaining operational simplicity, reaction stability, and excellent reproducibility.

Key words: Tandem cyclisation reaction, SNAr reaction, Aldol condensation, Quaternary carbon-containing fused indoline