Catalytic oxidation of 1,3-diisopropylbenzene using imidazolium ionic liquid as catalys

Korean Journal of Chemical Engineering

Volumn 26, Issue 4, 2009, Pages 985-989

  Xu, Shuai ^a   Huang, Chongpin ^a   Zhang, Jie ^a   Liu, Jia ^a   Chen, Biaohua ^a  

^a BEIJING UNIVERSITY OF CHEMICAL TECHNOLOGY   (China)

Author keywords

1,3 diisopropylbenzene; Catalysis; Hydroperoxide; Ionic liquid; Oxidation

Indexed keywords

EID: 70350141577     PISSN: 02561115     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11814-009-0163-1     Document Type: Article

References (33)

1. R. J. Schmidt, Appl. Catal. A, 280, 89 (2005).
2. C. Y. Wu and P. Pittsburgh, US Patent, 4,935,551 (1990).
3. H. S. Takaishi, I. D. Nishinomiya, T. C. Toyonaka, K. Tanimoto and H. Hosaka, US Patent, 3,953,521 (1976).
4. F. Minisci, F. Recupero, A. Cecchetto, C. Gambarotti, C. Punta and R. Paganelli, Org. Process Res. Dev., 8, 163 (2004).
5. F. G. Boyaí, S. Takaç and T. H. Özdamar, Appl. Catal. A, 172, 59 (1998).
6. O. Fukuda, S. Sakaguchi and Y. Ishii, Adv. Synth. Catal., 343, 809 (2001).
7. Y. Aoki, S. Sakaguchi and Y. Ishii, Adv. Synth. Catal., 346, 199 (2004).
8. Y. Ishii, S. Sakaguchi and T. Iwahama, Adv. Synth. Catal., 343, 393 (2001).
9. R. A. Sheldon and I. W. C. E. Arends, J. Mol. Catal. A, 251, 200 (2006).
10. F. Minisci, C. Punta and F. Recupero, J. Mol. Catal. A, 251, 129 (2006).
11. Y. Aoki, N. Hirai, S. Sakaguchi and Y. Ishii, Tetrahedron., 61, 10995 (2005).
12. T. Welton, Chem. Rev., 99, 2071 (1999).
13. R. Sheldon, Chem. Commun., 2399 (2001).
14. P. Wasserscheid and W. Keim, Angew. Chem. Int. Ed., 39, 3772 (2000).
15. R. D. Rogers and K. R. Seddon, Science, 302, 792 (2003).
16. H. Y. Ju, M. D. Manju, K. H. Kim, S. W. Park and D. W. Park, Korean J. Chem. Eng., 24, 917 (2007).
17. E. H. Lee, S. W. Cha, M. M. Dharma, Y. Choe, J. Y. Ahn and D. W. Park, Korean J. Chem. Eng., 24, 547 (2007).
18. N. Y. Mun, K. H. Kim, D. W. Park, Y. Choe and I. Kim, Korean J. Chem. Eng., 22, 556 (2005).
19. H. Y. Ju, J. Y. Ahn, M. D. Manju, K. H. Kim and D. W. Park, Korean J. Chem. Eng., 25, 471 (2008).
20. J. Muzart, Adv. Synth. Catal., 348, 275 (2006).
21. H. P. Zhu, F. Yang, J. Tang and M. Y. He, Green Chem., 5, 38 (2003).
22. G. Driver and K. E. Johnson, Green Chem., 5, 163 (2003).
23. K. R. Seddon and A. Stark, Green Chem., 4, 119 (2002).
24. C. P. Mehnert, N. C. Dispenziere and R. A. Cook, Chem. Commun., 1610 (2002).
25. L. M. Rossi, G. Machado, P. F. P. Fichtner, S. R. Teixeira and J. Dupont, Catal. Lett., 92, 149 (2004).
26. Q. X. Wan, Y. Liu, Y. Lu, M. Li and H. H. Wu, Catal. Lett., 121, 331 (2008).
27. B. C. Ranu and S. Banerjee, Org. Lett., 7, 3049 (2005).
28. J. M. Xu, C. Qiao, B. K. Liu, Q. Wu and X. F. Lin, Tetrahedron., 63, 986 (2007).
29. B.C. Ranu, S. Banerjee and R. Jana, Tetrahedron., 63, 776 (2007).
30. J. G. Huddleston, A. E. Visser, W. M. Reichert, H. D. Willauer, G. A. Broker and R. D. Rogers, Green Chem., 3, 156 (2001).
31. P. Bonhôte, A. P. Dias, N. Papageorgiou, K. Kalyanasundaram and M. Grätzel, Inorg. Chem., 35, 1168 (1996).
32. S. T. Handy and M. Okello, J. Org. Chem., 70, 1915 (2005).
33. C. Y. Wu, US Patent, 4,847,437 (1989).