Chin. J. Org. Chem. ›› 2017, Vol. 37 ›› Issue (6): 1501-1505.DOI: 10.6023/cjoc201610031 Previous Articles     Next Articles



付文强a, 谭平b, 邓伟a, 向建南a   

  1. a. 湖南大学化学化工学院化学生物传感与计量学国家重点实验室 长沙 410082;
    b. 湖南机电职业技术学院 长沙 410151
  • 收稿日期:2016-10-18 修回日期:2016-12-30 发布日期:2017-01-20
  • 通讯作者: 向建南
  • 基金资助:


Efficient Hydrolysis of Haloalkynes to α-Haloketones in Ionic Liquid

Fu Wenqianga, Tan Pingb, Deng Weia, Xiang Jiannana   

  1. a. State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering,Hunan University, Changsha 410082;
    b. Hunan Mechanical and Electrical Polytechnic, Changsha 410151
  • Received:2016-10-18 Revised:2016-12-30 Published:2017-01-20
  • Contact: 10.6023/cjoc201610031
  • Supported by:

    Project supported by the Planned Science and Technology Project of Hunan Province (No. 2015WK3003), the Scientific Research Fund of Hunan Provincial Education Department (No. 14C0405).

The haloalkynes were hydrolyzed to α-haloketones by sulfuric acid promotion in ionic liquids (ILs) with 85%~94% yields. The ILs-H2SO4 reaction system could be easily recycled (more five times) without any effect for reaction yield. At the same time, a wide scope of substrates haloalkynes were proper in this reaction system and a series of α-chloro/bromo/iodo acetophenones with different substituent (such as methyl, methoxyl, hydroxyl, nitro etc.) and aliphatic α-haloketones have been obtained in good yields.

Key words: ionic liquid, haloalkynes, hydration, α-haloketones, recyclable