Chinese Journal of Organic Chemistry ›› 2019, Vol. 39 ›› Issue (8): 2157-2165.DOI: 10.6023/cjoc201906005 Previous Articles     Next Articles

Special Issue: 陈茹玉先生诞辰100周年 元素有机化学合辑2018-2019



丛甜甜a, 王华敏a, 刘媛媛a, 吴海虹a, 张俊良a,b   

  1. a 华东师范大学化学与分子工程学院 上海市绿色化学与化工过程绿色化重点实验室 上海 200062;
    b 复旦大学化学系 上海 200438
  • 收稿日期:2019-06-06 修回日期:2019-07-09 发布日期:2019-07-17
  • 通讯作者: 刘媛媛, 吴海虹, 张俊良;;
  • 基金资助:


Phosphine-Mediated Sequential Staudinger/Aza-Michael Addition of Azides with Unsaturated Ketones to Synthesize β-Amino Substituted Ketones

Cong Tiantiana, Wang Huamina, Liu Yuanyuana, Wu Haihonga, Zhang Junlianga,b   

  1. a Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062;
    b Department of Chemistry, Fudan University, Shanghai 200438
  • Received:2019-06-06 Revised:2019-07-09 Published:2019-07-17
  • Contact: 10.6023/cjoc201906005;;
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21871088), the Chenguang Program supported by Shanghai Education Development Foundation and Shanghai Municipal Education Commission (No. 16CG22), and the Fundamental Research Funds for the Central Universities (No. 21871088).

A phosphine-mediated Staudinger/Aza-Michael addition of azides with trifluoromethyl substituted α,β-unsaturated ketones was developed, giving hydroamination products in medium to good yields (up to 96%). The hydroamination products could be prepared on gram scale and a wide range of substrates are tolerated under the optimized reaction conditions (30 examples). 31P NMR experiments indicate that this reaction was initiated by Staudinger reaction of azide with phosphine.

Key words: phosphines, Staudinger reaction, aza-Michael addition, azides, hydroamination, alkenes