有机化学 上一篇    下一篇

研究论文

多相铁催化环状醚C(sp3)-H键活化的芳基烯烃氧烷基化

于蕾a, 盛康b, 李亭a,*, 唐从辉b,*   

  1. a南阳师范学院化学与制药工程学院 南阳 473061;
    b能量转换与存储材料化学教育部重点实验室,材料化学与服役失效湖北省重点实验室,华中科技大学化学与化工学院 武汉 430074
  • 收稿日期:2023-12-22 修回日期:2024-02-01
  • 基金资助:
    国家自然科学基金(No. 22371083, 22001086)资助项目.

Heterogeneous Iron-Catalyzed Oxyalkylation of Vinylarenes via C(sp3)-H Activation of Cyclic Ethers

Lei Yua, Kang Shengb, Ting Lia,*, Conghui Tangb,*   

  1. aCollege of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nanyang, 473061;
    bKey Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan, 430074
  • Received:2023-12-22 Revised:2024-02-01
  • Contact: *E-mail: ctang@hust.edu.cn; chemlt2015@nynu.edu.cn
  • Supported by:
    National Natural Science Foundation of China (No. 22371083, 22001086).

烯烃双官能团化是一种重要的在双键上构建新的化学键的方法,烯烃的氧烷基化反应能够提供同时生成含有碳碳键和碳氧键的产物。然而当前的氧烷基化方法需要使用过氧叔丁醇作为氧化剂。因此,亟需发展一类需氧氧化体系的氧烷基化反应。我们在此报道一例温和条件下多相铁催化的苯乙烯及其衍生物的氧烷基化反应,使用空气作为氧化剂和氧源,本文进行了详细的催化剂表征、底物范围探索以及机理实验,并且给出了可能的机理过程。

关键词: 烯烃, 双官能团化, sp3碳氢键活化, 多相铁催化

Alkene difunctionalization is an important route to construct new chemical bonds across the olefin double bond, oxyalkylation reaction of olefins will provide C-C bond and C-O bond forming products. The current oxyalkylation methods rely in employing tert-butyl hydroperoxide as the oxidant. Therefore, developing an aerobic oxidation system for this transformation is highly desired. Herein, we report an unprecedented heterogeneous iron catalyst for oxyalkylation of styrene derivatives under mild conditions, air was used as the oxidant and oxygen source, detailed catalyst characterization, substrate scope and mechanistic studies were carried out and a proposed mechanism was given.

Key words: alkene, difunctionalization, C(sp3)-H activation, heterogeneous iron catalysis