The synthesis of 4,4′-arylmethylene-bis(3-(trifluoromethyl)-1-phenyl-1H-pyrazol-5-ol) in aqueous media without catalyst

Journal of Fluorine Chemistry

Volumn 128, Issue 2, 2007, Pages 105-109

  Yao, Chang Sheng ^a,b   Yu, Chen Xia ^a,b   Tu, Shu Jiang ^a,b   Shi, Da Qing ^a,b   Wang, Xiang Shan ^a,b   Zhu, You Quan ^c   Yang, Hua Zheng ^c  

^a JIANGSU NORMAL UNIVERSITY   (China)

^b JIANGSU NORMAL UNIVERSITY   (China)

^c NANKAI UNIVERSITY   (China)

Author keywords

1 Phenyl 3 trifluoromethylpyrazol 5 one; 4,4 Arylmethylene bis(3 (trifluoromethyl) 1 phenyl 1H pyrazol 5 ol); Aqueous media; Catalyst; Environment friendly

Indexed keywords

EID: 33846151663     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2006.10.006     Document Type: Article

References (36)

1. For recent advances, see:
2. KirK K.L. J. Fluorine Chem. 127 (2006) 1013-1029
3. Bégué J.-P., and Bonnet-Delpon D. J. Fluorine Chem. 127 (2006) 992-1012
4. Chambers R.D., Holling D., Sandforda G., Batsanov A.S., and Howard J.A.K. J. Fluorine Chem. 125 (2004) 661-671
5. Ramachandran P.V. Proceedings of the ACS Symposium Series. ACS, Washington, DC (2000)
6. Himaya T. Organofluorine Compounds (2001), Springer-Verlag, Berlin, Heidelberg
7. Kirsch P. Modern Fluoroorganic Chemistry: Synthesis, Reactivity and Applications (2004), Wiley-VCH, New York/Heidelberg
8. Ojima I., McCarthy J.R., and Welch J.T. Biomedical Frontiers of Fluorine Chemistry (1996), American Chemical Society, Washington, DC
9. Quan M.L., Lam P.Y.S., Han Q., Pinto D.J.P., He M.Y., Li R.H., Ellis C.D., Clark C.A., Sun J.H., Alexander R.S., Bai S., Luettgen J.M., Knabb R.M., Wong P.C., and Wexler R.R. J. Med. Chem. 48 (2005) 1729-1744
10. Khudina O.G., Shchegol'kov E.V., Burgart Ya.V., Kodess M.I., Kazheva O.N., Chekhlov A.N., Shilov G.V., Dyachenko O.A., Saloutin V.I., and Chupakhin O.N. J. Fluorine Chem. 126 (2005) 1230-1238
11. Schlosser M., Volle J.N., Leroux F., and Schenk K. Eur. J. Org. Chem. (2002) 2913-2920
12. Abid M., and Török B. Adv. Synth. Catal. 347 (2005) 1797-1803
13. O'Hagan S.C., Cobb S.L., Hamilton J.T.G., Cormac D., and Murphy C.D. Nature 416 (2002) 279
14. Park H.-J., Lee K., Park S.-J., Ahn B., Lee J.-C., Cho H.Y., and Lee K.-I. Bioorg. Med. Chem. Lett. 15 (2005) 3307-3312
15. Clark M.P., Laughlin S.K., Laufersweiler M.J., Bookland R.G., Brugel T.A., Golebiowski A., Sabat M.P., Townes J.A., VanRens J.C., Djung J.F., Natchus M.G., De B., Hsieh L.C., Xu S.C., Walter R.L., Mekel M.J., Heitmeyer S.A., Brown K.K., Juergens K., Taiwo Y.O., and Janusz M.J. J. Med. Chem. 11 (2004) 2724-2727
16. I.H. Cho, J.Y. Noh, S.W. Park, H.C. Ryu, J.W. Lim, J.H. Kim, M.Y. Chae, D.H. Kim, S.H. Jung, H.J. Park, Y.H. Kim, I.K. Min, US Patent 2 004 002 532 (2004).
17. M.P. Clark, S.K. Laughlin, A. Golebiowski, T.A. Brugel, M. Sabat, WO Patent 2 005 047 287 (2005).
18. Yasutaka K., Narie S., Mieko S.-M., Hiromu M., and Kimiko M.-M. Biochem. Biophys. Res. Commun. 4 (2004) 1351-1358
19. Clark M.P., and Bookland R.G. Expert Opin. Ther. Pat. 11 (2005) 1617-1623
20. M. Ishida, WO Patent 2 006 006 212 (2006).
21. M. Speckbacher, H.-J. Braun, WO Patent 2 006 012 934 (2006).
22. Takeishi H., Kitatsuji Y., Kimura T., Meguro Y., Yoshida Z., and Kihara S. Anal. Chim. Acta 1 (2001) 69-80
23. Abdel-Latif S.A. Synth. React. Inorg. Metal-organic Chem. 8 (2001) 1355-1374
24. Pettinari C., Marchetti F., Pettinari R., Martini D., Drozdov A., and Troyanov S. J. Chem. Soc., Dalton Trans. 11 (2001) 1790-1797
25. Buzykin B.I., and Lonshchakova T.I. Russ. Chem. Bull. 10 (1971) 2224-2226
26. Li X.-L., Ma H., Wang Y.-M., and Meng J.-B. Chem. J. Chin. Univ. 12 (1995) 1903-1906 (in Chinese)
27. Bai Y.-J., Lu J., Wang Z.-J., Gan H.-Y., and Ma H.-R. Chin. J. Org. Chem. 6 (2004) 616-620 (in Chinese)
28. DeSimone J.M. Science 5582 (2002) 799-803
29. For recent advances, see:
30. Andrade C.K.Z., and Alves L.M. Curr. Org. Chem. 2 (2005) 195-218
31. Pirrung M.C. Chem. Eur. J. 5 (2006) 1312-1317
32. Li C.-J. Chem. Rev. 8 (2005) 3095-3165
33. Shi D.-Q., Chen J., Wu N., Zhuang Q.-Y., and Wang X.-S. Chin. J. Org. Chem. 4 (2005) 405-408
34. Wang W., Wang S.-X., Qin X.-Y., and Li J.-T. Synth. Commun. 9 (2005) 1263-1269
35. Mao C.-H., Lu Y.-F., Huang M.-Z., Huang L., Chen C., and Ou X.-M. Chin. J. Syn. Chem. 2 (2002) 167-169
36. SHELXTL (Version 5.1). Bruker AXS Inc., Madison, Wisconsin, USA.