Catalysis Letters

, Volume 132, Issue 1–2, pp 16–21 | Cite as

A Novel Transfer Hydrogenation with High Hydrogen Utilization for the Hydrogenation of Halogenated Nitrobenzene without Hydrodehalogenation

Article

Abstract

In the novel catalytic transfer hydrogenation, 12 active hydrogen (H*) can be transferred from water/ethanol system as the efficient hydrogen donor and used directly for the hydrogenation of halogenated nitrobenzene over Ru–Fe/C catalyst, obtaining o-chloroaniline (o-CAN) with 98.0% selectivity at 99.8% conversion without hydrodehalogenation. Most other halogenated nitrobenzenes were reduced with selectivity >98%, and conversion >99.0%. Moreover, the Ru–Fe/C catalyst was still active after reaction for 480 h.

Keywords

Aqueous-phase reforming Ru–Fe/C Catalytic transfer hydrogenation Halogenated nitrobenzene 

Notes

Acknowledgments

This work was supported by the National Natural Science Foundation of China (20676124).

References

  1. 1.
    Rao PS, Anand J, Palaniappan S, Sathyanarayana DN (2000) Eur Polym J 36:915CrossRefGoogle Scholar
  2. 2.
    Ding Y, Boone HW, Anderson JD, Padias AB, Hall HK (2001) Macromolecules 34:5457CrossRefGoogle Scholar
  3. 3.
    Surrey AR, Hammer HF (1946) J Am Chem Soc 68:113CrossRefGoogle Scholar
  4. 4.
    Johnstone RAW, Wilby AH (1985) Chem Rev 85:129CrossRefGoogle Scholar
  5. 5.
    Brieger G, Nestrick TJ (1974) Chem Rev 74:567CrossRefGoogle Scholar
  6. 6.
    Zassinovich G, Mestroni G, Gladiali S (1992) Chem Rev 92:1051CrossRefGoogle Scholar
  7. 7.
    Channe GD, Mahesh B (2000) Syn Commun 30:3639CrossRefGoogle Scholar
  8. 8.
    Kulkarni AS, Jayaram RV (2004) J Mol Catal A 223:107CrossRefGoogle Scholar
  9. 9.
    Chaubal NS, Sawant MR (2007) J Mol Catal A 261:232CrossRefGoogle Scholar
  10. 10.
    Tafesh AM, Weiguny J (1996) Chem Rev 96:2035CrossRefGoogle Scholar
  11. 11.
    Naota T, Takaya H, Murahashi SI (1998) Chem Rev 98:2599CrossRefGoogle Scholar
  12. 12.
    Llorca J, de la Piscina PR, Sales J, Homs NS (2001) Chem Commun 641Google Scholar
  13. 13.
    Deluga GA, Salge JR, Schmidt LDJ (2004) Sci 303:993CrossRefGoogle Scholar
  14. 14.
    Liu LQ, Qiao BT, Chen ZJ, Zhang J, Deng YQ (2009) Chem Commun 653Google Scholar
  15. 15.
    Fatsikostas AN, Kondarides DI, Verykios XE (2001) Chem Commun 851Google Scholar
  16. 16.
    Fatsikostas AN, Dl Kondarides, Verykios XE (2003) Catal Today 75:145CrossRefGoogle Scholar
  17. 17.
    Yan XH, Sun JQ, Wang YW, Yang JF (2006) J Mol Catal A 252:17CrossRefGoogle Scholar
  18. 18.
    Coq B, Tijani A, Dutartre R, Figuéras F (1991) Appl Catal 76:255CrossRefGoogle Scholar
  19. 19.
    Menini C, Park C, Shin E, Tavoularis G, Keane M (2000) Catal Today 62:355CrossRefGoogle Scholar

Copyright information

© Springer Science+Business Media, LLC 2009

Authors and Affiliations

  1. 1.State Key Laboratory Breeding Base of Green Chemistry-Synthesis TechnologyZhejiang University of TechnologyHangzhouPeople’s Republic of China

Personalised recommendations