Chin. J. Org. Chem. ›› 2018, Vol. 38 ›› Issue (6): 1538-1543.DOI: 10.6023/cjoc201802019 Previous Articles     Next Articles

Special Issue: 镍催化有机反应合辑



张刚, 杓学蓓, 李清寒, 杨学军   

  1. 西南民族大学化学与环境保护工程学院 成都 610041
  • 收稿日期:2018-02-14 修回日期:2018-04-04 发布日期:2018-05-17
  • 通讯作者: 李清寒,
  • 基金资助:


Synthesis of Symmetrical 1, 3-Diynes via Cross-Coupling Reaction of Alkynyl Bromide with Alkynyl Aluminum Catalyzed by Nickel

Zhang Gang, Shao Xuebei, Li Qinghan, Yang Xuejun   

  1. College of Chemistry and Environmental Protection Engineering, Southwest Minzu University, Chengdu 610041
  • Received:2018-02-14 Revised:2018-04-04 Published:2018-05-17
  • Contact: 10.6023/cjoc201802019
  • Supported by:

    Project supported by the Postgraduate Degree Construction Project of Southwest University for Nationalities (No. CX2016SZ063) and the Sichuan Provincial Department of Science and Technology Support Program (No. 2015NZ0033).

1,3-Diyne compounds are important inter mediates in organic synthesis, which are widely used in pharmaceutical chemistry, organic synthesis and materials science. A highly efficient for the synthesis of 1,3-diyne via cross-coupling of alkynyl bromides with alkynyl aluminium reagents catalyzed by nickel has been developed. The coupling reaction of alkynyl bromides with alkynyl aluminium reagents mediated by Ni(acac)2 (5 mol%)/1,2-bis(diphenylphosphino)ethane nickel(Ⅱ) chloride (DPPE) (10 mol%)in 1,2-dimethoxyethane afforded the corresponding coupling products 1,3-diyne in good to excellent yields(up to 90%) at room temperature for 5 h. The coupling reaction of alkynyl aluminum with different substituents and alkynyl bromine with various substituents can afforded the coupling products in good yields. Importantly, the α-ethynylnaphthalene and 2-ethynylthiophene were also suitable for the reaction. This process is simple and easily performed, which provides an efficient method for the synthesis of 1,3-diynes derivatives.

Key words: 1,3-diyne, nickel, alkynyl bromide, alkynyl aluminium, cross-coupling