研究简报

双缩二氨基硫脲席夫碱锰配合物催化Henry反应的研究

  • 张鹏 ,
  • 何军 ,
  • 万宁宁 ,
  • 张维东 ,
  • 惠永海 ,
  • 解正峰
展开
  • a 石油天然气精细化工教育部&新疆维吾尔自治区重点实验室 新疆大学化学化工学院 乌鲁木齐 830046;
    b 中国石油独山子石化公司炼油厂 独山子 833600

收稿日期: 2013-01-22

  修回日期: 2013-03-23

  网络出版日期: 2013-04-07

基金资助

国家自然科学基金(Nos. 21262034, 20962018, 20862015, 20562011)资助项目.

Bis-thiocarbohydrazones Schiff Base Mn(II) Complex as a Catalyst for Henry Reaction

  • Zhang Peng ,
  • He Jun ,
  • Wan Ningning ,
  • Zhang Weidong ,
  • Hui Yonghai ,
  • Xie Zhengfeng
Expand
  • a Key Laboratory of Oil & Gas Fine Chemicals, Ministry of Education & Xinjiang Uyghur Autonomous Region, College of Chemistry and Chemical Engineering, Urumqi 830046;
    b Oil Refinery of Petrochina Dushanzi Petrochemical Company, Dushanzi 833600

Received date: 2013-01-22

  Revised date: 2013-03-23

  Online published: 2013-04-07

Supported by

Project supported by the National Natural Science Foundation of China (Nos. 21262034, 20962018, 20862015, 20562011).

摘要

在室温下用双缩二氨基硫脲席夫碱锰(II)配合物催化了醛和硝基甲烷的Henry反应, 方便有效地合成了一系列的β-硝基醇. 具有反应条件温和、操作简单、产率高、催化剂用量少、且对环境友好等优点.

本文引用格式

张鹏 , 何军 , 万宁宁 , 张维东 , 惠永海 , 解正峰 . 双缩二氨基硫脲席夫碱锰配合物催化Henry反应的研究[J]. 有机化学, 2013 , 33(08) : 1834 -1838 . DOI: 10.6023/cjoc201301055

Abstract

Bis-thiocarbohydrazones Schiff base Mn(II) complex catalyzes the Henry reaction between aldehydes and nitromethane to afford β-nitroalcohol derivatives at room temperature. The remarkable advantages of this reaction were mild reaction conditions, simple workup procedure, high yield of products, less catalyst and environmental friendly.

参考文献

[1] Luzzio, F. A. Tetrahedron 2001, 57, 915.
[2] Anbazhagan, M.; Kumaran, G.; Sasidharan, M. J. Chem. Res., Synop. 1997, 336.
[3] Watanabe, M.; Murata, K.; Ikariya, T. J. Org. Chem. 2002, 67, 1712.
[4] Ballini, R.; Boscia, G. J. Org. Chem. 1994, 59, 5466.
[5] Alvarez-Casao, Y.; Marques-Lopez, E.; Herrera, R. P. Symmetry 2011, 3, 220.
[6] Du, D. M.; Lu, S. F.; Fang, T.; Xu, J. X. J. Org. Chem. 2005, 70, 3712.
[7] Trost, B. M.; Yeh, V. S. C. Angew. Chem. 2002, 114, 889.
[8] Sasai, H.; Suzuki, T.; Arai, S.; Arai, T.; Shibasaki, M. J. Am. Chem. Soc. 1992, 114, 4418.
[9] Sohtome, Y.; Hashimoto, Y.; Nagasawa, K. Adv. Synth. Catal. 2005, 347, 1643.
[10] Wang, X.; Fang, F.; Tian, S. K. Tetrahedron Lett. 2008, 49, 6442.
[11] Pandeya, S. N.; Sriram, D.; Nath, G.; Clercq, E. D. Farmaco 1999, 54, 624.
[12] Drozdzak, R.; Allaert, B.; Ledoux, N.; Dragutan, I.; Dragutan, V.; Verpoort, F. Coord. Chem. Rev. 2005, 249, 3055.
[13] Yamada, S. Coord. Chem. Rev. 1999, 190192, 537.
[14] Xie, Z. F.; Zhang, J. Z.; Liu, F. M. Chin. J. Org. Chem. 2011, 31, 548 (in Chinese).
(解正峰, 张建中, 刘方明, 有机化学, 2011, 31, 548.)
[15] Meng, H.; Xie, Z. F.; Hu, J.; Liu, F. M. Chin. J. Org. Chem. 2008, 28, 1423 (in Chinese).
(孟华, 解正峰, 胡君, 刘方明, 有机化学, 2008, 28, 1423.)
[16] Zhou, G. P.; Hui, Y. H.; Wan, N. N.; Liu, Q. J; Xie, Z. F.; Wang, J. D. Chin. Chem. Lett. 2012, 23, 690.
[17] Wan, N. N.; Hui, Y. H.; Xie, Z. F.; Wang, J. D. Chin. J. Chem. 2012, 30, 311.
[18] Hui, Y. H.; Chen, C. M.; Xie, Z. F. Chin. Chem. Lett. 2012, 23, 525.
[19] Chen, Y. C.; Chen, Y. Y.; Xie, Z. F.; Wang, W. P. Chin. J. Org. Chem. 2011, 31, 1672 (in Chinese).
(陈永诚, 陈圆圆, 解正峰, 王文平, 有机化学, 2011, 31, 1672.)
[20] Boruwa, J.; Gogoi, N.; Saikia, P. P.; Barua, N. C. Tetrahedron: Asymmetry 2006, 17, 3315.
[21] Li, Z. G.; Wang, Q. M.; Huang, J. M. Preparation of Organic Intermediates, 2nd ed., Chemical Industry Press, Beijing, 1996, pp. 152~153 (in Chinese).
(李在国, 汪清民, 黄君珉, 有机中间体制备, 第2版, 化学工业出版社, 北京, 1996, pp. 152~153.)
文章导航

/