研究论文

5-三氟甲基胡椒醛的合成研究

  • 王亚虎 ,
  • 韩民 ,
  • 张兰兰 ,
  • 周水平 ,
  • 段中余
展开
  • a 河北工业大学化工学院 天津 300130;
    b 天津天士力集团研究院现代中药研究所 天津 300410

收稿日期: 2012-11-07

  修回日期: 2012-12-21

  网络出版日期: 2013-01-07

基金资助

天津市科技支撑计划重点(No. 12ZCZDSY01200)、河北省自然科学基金(No. B2010000039)、河北省教育厅高等学校科学研究(No. 2011121)和教育部归国留学基金(2012)资助项目.

Studies on the Synthesis of 5-Trifluoromethylpiperonal

  • Wang Yahu ,
  • Han Min ,
  • Zhang Lanlan ,
  • Zhou Shuiping ,
  • Duan Zhongyu
Expand
  • a School of Chemical Engineering and Technology, Hebei University of Technology, Tianjin 300130;
    b Institute of Modern Tradtional Chinese Medicine, Institute of Tasly Academy, Tianjin Tasly Group Co. Ltd., Tianjin 300410

Received date: 2012-11-07

  Revised date: 2012-12-21

  Online published: 2013-01-07

Supported by

Project supported by Key Projects in the Tianjin Science & Technology Pillar Program (No. 12ZCZDSY01200), the Hebei Provincial Natural Science Foundation of China (No. B2010000039), the Hebei Education Department Research Project (No. 2011121) and the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry.

摘要

以香草醛为起始原料, 经碘代、脱甲基、亚甲基醚化、三氟甲基化反应以较高收率合成了5-三氟甲基胡椒醛, 产物结构经过了1H NMR, 13C NMR, 19F NMR和HRMS的确证. 重点研究了三氟甲基化反应, 考察了不同三氟甲基化试剂、溶剂、催化剂用量、反应温度以及反应时间对三氟甲基化反应收率的影响, 确定了最佳反应条件. 随后, 该方法成功运用于3, 4位不同取代的5-碘苯甲醛的三氟甲基化反应, 制得了三种5-三氟甲基胡椒醛的衍生物.

本文引用格式

王亚虎 , 韩民 , 张兰兰 , 周水平 , 段中余 . 5-三氟甲基胡椒醛的合成研究[J]. 有机化学, 2013 , 33(05) : 1057 -1061 . DOI: 10.6023/cjoc201211010

Abstract

5-Trifluoromethylpiperonal was obtained by iodination, demethylation, methylene etherification and trifluoromethyl reaction of vanillin in a satisfied yield. The chemical structure of the product was identified by 1H NMR, 13C NMR, 19F NMR and HRMS. The optimal reaction conditions were investigated, including trifluoromethylation reagents, solvents, catalyst amounts, reaction temperature and reaction time. Meanwhile, three hydroxy substituted derivatives of 3,4-dihydroxy- 5-iodo-benzaldehyde were acquired by trifluoromethylation reaction with this method.

参考文献

[1] Luo, M.; Ma H.-Z.; Su. Q.-D.; Li, Q.-R. Chin J. Struct. Chem. 2002, 21, 538.
[2] Yang, D.-Q.; Lv, F.; Li, W.-H.; Jiang, Q.-J.; Guo, W. Chin. J. Org. Chem. 2004, 24, 1465 (in Chinese).
(杨定乔, 吕芬, 李文辉, 蒋启军, 郭维, 有机化学, 2004, 24, 1465).
[3] Müller, K.; Faeh, C.; Diederich, F. Science. 2007, 317, 1881.
[4] Jiang, H.-Z.; Song, L.-P.; Luo, H.-H.; Yi, H.; Zhu, S.-Z.; Hao, J. J. Shanghai Univ. (Nat. Sci. Ed.) 2011, 17, 458 (in Chinese).
(蒋海珍, 宋力平, 罗会华, 易海, 朱仕正, 郝健, 上海大学学报(自然科学版), 2011, 17, 458.)
[5] Nie, J.; Guo, H.-C.; Cahard, D.; Ma, J.-A. Chem. Rev. 2011, 111, 455.
[6] Shinde, A. T.; Zangade, S. B.; Chavan, S. B. A. Synth. Commun. 2010, 40, 3506.
[7] Chen, X.; Qiao, X.; Cui, M.-F.; Zhang, J.-P.; Tang, J.-H. New Chem. Mater. 2005, 33, 63 (in Chinese).
(陈献, 乔旭, 崔咪芬, 张进平, 汤吉海, 化工新型材料, 2005, 33, 63.)
[8] Lei, H.; Zhu, H.-J.; Han, B.-Y.; Xu, S.-L. Fine Chem. 2004, 21, 639 (in Chinese).
(雷宏, 朱红军, 韩邦友, 徐守林, 精细化工中间体, 2004, 21, 639.)
[9] Qing, F.-L. Chin. J. Org. Chem. 2012, 32, 815 (in Chinese).
(卿凤翎, 有机化学, 2012, 32, 815.)
[10] Furuya, T.; Kamlet, A. S.; Ritter, T. Nature 2011, 473, 470.
[11] Chang, Y.; Cai, C. Tetrahedron Lett. 2005, 46, 3161.
[12] Markovich, K. M.; Tantishaiyakul, V.; Hamada, A.; Miller D. D.; Romstedt, K. J.; Shams G.; Shin Y.; Fraundorfer, P. F.; Doyle K.; Feller, D. R. J. Med. Chem. 1992, 35, 466.
[13] Chen, Q-Y,; Duan, J-X.;. Tetrahedron Lett. 1993, 34, 4241.
[14] Achelle, S.; Ple, N.; Turck, A.; Bouillon, J. P.; Portella, C. J. Heterocycl. Chem. 2006, 43, 1243.
[15] Bentley, J. M.; Adams D. R.; Bebbington, D.; Benwell, K. R.; Bickerdike, M. J.; Davidson, J. E. P.; Dawson, C. E.; Dourish, C. T.; Duncton, M. A. J.; Gaur, S.; George, A. R.; Giles, P. R.; Hamlyn, R. J.; Kennett, G. A.; Knight, A. R.; Malcolm, C. S.; Mansell, H. L.; Misra, A.; Monck, N. J. T.; Pratt, R. M.; Quirk, K.; Roffey, J. R. A.; Vickers, S. P.; Cliffe, I. A. Bioorg. Med. Chem. Lett. 2004, 14, 2367.
[16] Chen, Q.-Y. J. Fluorine Chem. 1995, 72, 241.
[17] Wu, T. R.; Shen, L.; Chong, J. M. Org. Lett. 2004, 6, 2701.
[18] Bueno, A. B.; Flynn, C. J.; Gilmore, J.; Marcos, A.; Montero, C.; Porterc, W.; Williamsb. A. C. Tetrahedron Lett. 2005, 46, 7769.
[19] Chen, Q.-Y.; Wu, S.-W. J. Chem. Soc., Chem. Commun. 1989, 705.
[20] Liu, C.; Chen, Q.-Y. Eur. J. Org. Chem. 2005, 3680.
[21] Roy, S.; Gregg, B. T.; Gribble, G. W.; Le, V. D.; Roy, S. Tetrahedron 2011, 67, 2161.
[22] Corbett, R. E.; Mcdowall, M. A. J. Chem. Soc., 1958, 3740.
[23] Anhoury, M. L.; Crooy, P.; Neys, R. D.; Eliaers, J. J. Chem. Soc., Perkin Trans. 1 1974, 1015.
[24] Nammalwar, B.; Bunce, R. A.; Berlin, K. D.; Bourne, C. R.; Bourne, P. C.; Barrow, E. W.; Barrow, W. W. Org. Prep. Proced. Int. 2012, 44, 146.
[25] Backstrom, R.; Honkanen, E.; Pippuri, A.; Kairisalo, P.; Pystynen, J.; Heinola, K.; Nissinen, E.; Linden, I. B.; Mannisto, P. T.; Kaakkla, S.; Pohto, P. J. Med. Chem. 1989, 32, 841.
文章导航

/