Chin. J. Org. Chem. ›› 2019, Vol. 39 ›› Issue (2): 555-560.DOI: 10.6023/cjoc201807017 Previous Articles     Next Articles



张硕a, 彭丹a, 赵宁a, 于一涛a, 王峰a, 刘海龙b, 伊港b   

  1. a 齐鲁工业大学(山东省科学院)山东省科学院新材料研究所 山东省特种含硅新材料重点实验室 济南 250014;
    b 山东东岳有机硅材料股份有限公司 淄博 256401
  • 收稿日期:2018-07-09 修回日期:2018-08-26 发布日期:2018-09-10
  • 通讯作者: 伊港
  • 基金资助:


Sc(OTf)3 Catalyzed Oxo-Michael Addition to o-Quinone Methides by Alcohols

Zhang Shuoa, Peng Dana, Zhao Ninga, Yu Yitaoa, Wang Fenga, Liu Hailongb, Yi Gangb   

  1. a Shandong Provincial Key Laboratory for Special Silicone-Containing Materials, Advanced Materials Institute, Qilu University of Technology(Shandong Academy of Sciences), Jinan 250014;
    b Shandong Dongyue Organosilicon Materials Co., Ltd., Zibo 256401
  • Received:2018-07-09 Revised:2018-08-26 Published:2018-09-10
  • Contact: 10.6023/cjoc201807017
  • Supported by:

    Project supported by the Shandong Provincial Natural Science Foundation (No. ZR2017BB033), the Youth Science Funds of Shandong Academy of Sciences (No. 2018QN0030) and the National Natural Science Foundation of China (No. 51503118).

o-Quinone derivatives are not only a variety of active and important intermediate, but also widely used in the synthesis of natural products and medicinal chemistry. In the present study, the Sc(OTf)3 catalyzed oxo-Michael addition to o-quinone methides by alcohols was developed. The products were obtained in moderate to good yields (76%~97%) under mild conditions. Furthermore, the reaction could be scaled up to multigram scale.

Key words: o-quinone, scandium(III) triflate, oxo-Michael addition, green chemistry