研究论文

钯催化下α-溴代腈与末端烯烃的Heck型偶联反应

  • 班银 ,
  • 杨建 ,
  • 杨莎莎 ,
  • 满雪玉 ,
  • 黄洋
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  • a遵义医科大学药学院 贵州省化学药物创制全省重点实验室 贵州遵义 563003;
    b湖南医药学院药学院 湖南怀化 418000

收稿日期: 2026-06-12

  修回日期: 2026-06-30

  网络出版日期: 2026-09-08

基金资助

遵义医科大学 (No. F-1119)资助项目.

Palladium-Catalyzed Heck-Type Reaction of α-Bromonitriles with Terminal Alkenes

  • Ban Yin ,
  • Yang Jian ,
  • Yang Shasha ,
  • Man Xueyu ,
  • Huang Yang
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  • aGuizhou Provincial Key Laboratory of Innovation and Manufacturing for Pharmaceuticals,School of Pharmacy, Zunyi Medical University, Zunyi, 563003;
    bSchool of Pharmaceutical Sciences, Hunan University of Medicine, Huaihua, Hunan, 418000

Received date: 2026-06-12

  Revised date: 2026-06-30

  Online published: 2026-09-08

Supported by

Zunyi Medical University (No. F-1119).

摘要

α-溴代腈是一类重要的合成砌块,被应用于合成含有氰基烷基结构的化合物中。然而,其在过渡金属钯催化下的偶联反应尚未有研究。该反应体系面临两个关键的问题:其一,α-溴代腈可能会与钯配位,从而影响催化效率;其次,该底物易发生β-氢消除副反应。针对上述挑战,本研究发展了α-溴代腈与末端烯烃在钯催化下的Heck偶联反应。该反应条件温和、操作简便,具有良好官能团兼容性和广泛的底物普适性。此外,该方法也适用于药物分子的后期官能团化修饰,展示出了良好的合成应用潜力。

本文引用格式

班银 , 杨建 , 杨莎莎 , 满雪玉 , 黄洋 . 钯催化下α-溴代腈与末端烯烃的Heck型偶联反应[J]. 有机化学, 2026 : 202603018 . DOI: 10.6023/cjoc202603018

Abstract

α-Bromonitriles represented an important synthetic building block. They have been used to prepare compounds containing cyanoalkyl groups. However, their coupling reactions under palladium catalysis remains unexplored. This reaction presents two challenges: firstly, α-bromonitriles may coordinate with palladium and lower its catalytic activity. Second, they tend to undergo β-hydrogen elimination. To solve these problems, we developed a palladium-catalyzed Heck coupling between α-bromonitriles and terminal alkenes. This operationally simple protocol proceeds under mild conditions, and exhibits broad functional group compatibility as well as a wide substrate scope. Furthermore, the method is applicable to the late-stage functionalization of pharmaceutical molecules, demonstrating its potential for synthetic applications.

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