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Facile dehalogenation of halogenated anilines and their derivatives using Al-Ni alloy in alkaline aqueous solution

  • Research Article
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Central European Journal of Chemistry

Abstract

This article describes the simple hydrodehalogenation of halogenated anilines and their derivatives by the action of Raney aluminium-nickel alloy in aqueous alkaline solution at room temperature. The reaction course was monitored by means of 1H nuclear magnetic resonance (NMR) spectroscopy and GC-MS spectra.

The effect of Al and Ni and the nature and quantity of the base for effective hydrodehalogenation were studied.

The possibility of lowering Al content more than 500 times and Ni content more than 10 times in the filtered mother liquor by a dehalogenation procedure was tested using precipitation.

The reduction method described was satisfactorily proved for dehalogenation of polyhalogenated anilines in the multiphase dimethoxymethane/aqueous NaOH/Al-Ni reaction mixture. Dehalogenation under multi-phase conditions was demonstrated for the preparation of ortho-alkylated anilines from simply available 2-substituted-4-chloroanilines.

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References

  1. F. Effenberger, Angew. Chem., Int. Ed. 41, 1699 (2002)

    Article  CAS  Google Scholar 

  2. V.V. Grushin, Acc. Chem. Res. 26, 279 (1993)

    Article  CAS  Google Scholar 

  3. H.Y. Choi, D.Y. Chi, J. Am. Chem. Soc. 123, 9202 (2001)

    Article  CAS  Google Scholar 

  4. M.H. Block, S. Boyer, W. Brailsford, D.R. Brittain, D. Carroll, S. Chapman, D.S Clarke, C.S. Donald, K.M. Foote, L. Godfrey, A. Ladner, P.R. Marsham, D.J. Masters, C.D. Mee, M.R. O’Donovan, J.E. Pease, A.G. Pickup, J.W. Roberts, A. Rayner, P. Schofield, A. Suleman, A.V. Turnbull, J. Med. Chem. 45, 3509 (2002)

    Article  CAS  Google Scholar 

  5. The Merck Index, An Encyclopedia of Chemicals, Drugs and Biologicals (Merck&Co., Inc., NI-159, New York, 1996) 640, 1209, 1239

    Google Scholar 

  6. E.C. Cortés, R.S. Franco, O.G. Mellado, J. Heterocyclic Chem. 38, 663 (2001)

    Article  Google Scholar 

  7. L.T. Kaspar, B. Fingerhut, L. Ackermann, Angew. Chem., Int. Ed. 44, 5972 (2005)

    Article  CAS  Google Scholar 

  8. N. Seshu Babu, K. Mohan Reddy, P.S. Sai Prasad, I. Suryanarayana, N. Lingaiah, Tetrahedron Lett. 48, 7642 (2007)

    Article  CAS  Google Scholar 

  9. A. Arienti, F. Bigi, R. Maggi, E. Marzi, P. Moggi, Tetrahedron 53, 3795 (1997)

    Article  CAS  Google Scholar 

  10. X.-T. Huang, Z.-Y. Long, Q.-Y. Chen, J. Fluorine Chem. 111, 107 (2001)

    Article  CAS  Google Scholar 

  11. S.H. Yalkowsky, Y. He, Handbook of Aqueous Solubility Data (CRC Press, Boca Raton, Florida, 2003) 244

    Book  Google Scholar 

  12. C. Tixier, M. Sancelme, F. Bonnemoy, A. Cuer, N. Truffaut, H. Veschambre, Environ. Toxicol. Chem. 20, 1381 (2001)

    Article  CAS  Google Scholar 

  13. F. Massicot, R. Schneider, Y. Fort, S. Illy-Cherrey, O. Tillement, Tetrahedron 56, 4765 (2000)

    Article  CAS  Google Scholar 

  14. F. Alonso, I.P. Beletskaya, M. Yus, Chem. Rev. 102, 4009 (2002)

    Article  CAS  Google Scholar 

  15. G.-B. Liu, H.-Y. Zhao, B. Yang, T. Thiemann, Green Chem. Lett. Rev. 3, 1 (2010)

    Article  CAS  Google Scholar 

  16. V. Dichiarante, M. Fagnoni, A. Albini, Green Chem. 11, 942 (2009)

    Article  CAS  Google Scholar 

  17. X. Xu, H. Zhou, M. Zhou, Chemosphere 62(5), 847 (2006)

    Article  CAS  Google Scholar 

  18. G. Lunn, E.B. Sansone, AIHA Journal 52, 252 (1991)

    Article  CAS  Google Scholar 

  19. L.K. Keefer, G. Lunn, Chem. Rev. 89, 459 (1989)

    Article  CAS  Google Scholar 

  20. G.-B. Liu, L. Dai, X. Gao, M.-K. Li, T. Thiemann, Green Chem. 8, 781 (2006)

    Article  CAS  Google Scholar 

  21. G.-B. Liu, L. Dai, X. Gao, M.K. Li, T. Thiemann, Tetrahedron 65(12), 2497 (2009)

    Article  CAS  Google Scholar 

  22. T. Weidlich, A. Krejčová, L. Prokeš, Monats. Chem. 141, 1015 (2010)

    Article  CAS  Google Scholar 

  23. A.H.M. Veeken, W.H. Rulkens, Water Sci. Technol. 47(10), 9 (2003)

    CAS  Google Scholar 

  24. T.S. Roetting, J. Cama, C. Ayora, J.L. Cortina, J. De Pablo, Environ. Sci. Technol. 40, 6438 (2006)

    Article  CAS  Google Scholar 

  25. J.Y. Lee, S.V. Rao, B.N. Kumar, D.J. Kang, B.R. Reddy, J. Hazard. Mater. 176, 1122 (2010)

    Article  CAS  Google Scholar 

  26. A. Agueera, E. Almansa, A. Tejedor, A.R. Fenrandez-Alba, S. Malato, M.I. Maldonado, Environ. Sci. Technol. 34, 1563 (2000)

    Article  CAS  Google Scholar 

  27. D. Quo, H. Huang, H. Jiang, H. Liu, J. Xu, Org. Lett. 10, 4513 (2008)

    Article  Google Scholar 

  28. G. Manolikates, M.A. Schade, A. Metzger, P. Knochel, C. Munoz Hernandez, J. Org. Chem. 73, 8422 (2008)

    Article  Google Scholar 

  29. M. Tordeux, B. Langlois, C.J. Wakselman, Chem. Soc., Perkin Trans. 1,8, 2293 (1990)

    Google Scholar 

  30. C.R. Gannelin, D.J. Triggle, Dictionary of pharmacological agents 1–2 (Chapman and Hall, London, 1996) 663

    Google Scholar 

  31. G.-B. Liu, H.-Y. Zhao, B. Yang, T. Thiemann, Green Chem. Lett. Rev. 3, 1 (2010)

    Article  CAS  Google Scholar 

  32. B.H. Lipschutz, S. Tasler, Adv. Synth. Catal. 343, 327 (2001)

    Article  Google Scholar 

  33. T. Janiak, J. Blazejowski, Chemosphere 48,1097 (2002)

    Article  CAS  Google Scholar 

  34. C.J.H. Miermans, L.E. van der Velde, P.C.M. Frintrop, Chemosphere 40, 39 (2000)

    Article  CAS  Google Scholar 

  35. W. Tsuzuki, A. Ue, A. Nagao, Biosci. Biotechnol. Biochem. 67, 1660 (2003)

    Article  CAS  Google Scholar 

  36. H.E. Seifried, R.M. Seifried, J.J. Clarke, T.B. Junghans, R.H.C. San, Chem. Res. Toxicol. 19, 627 (2006)

    Article  CAS  Google Scholar 

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Correspondence to Tomáš Weidlich.

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Weidlich, T., Prokeš, L. Facile dehalogenation of halogenated anilines and their derivatives using Al-Ni alloy in alkaline aqueous solution. cent.eur.j.chem. 9, 590–597 (2011). https://doi.org/10.2478/s11532-011-0033-7

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  • DOI: https://doi.org/10.2478/s11532-011-0033-7

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