A green and efficient oxidation of benzylic alcohols using H2O2 catalyzed by Montmorillonite-K10 supported MnCl2

Chinese Chemical Letters

Volumn 21, Issue 10, 2010, Pages 1162-1164

  Najafi, Gholam Reza ^a  

^a ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

Green oxidation system; Hydrogen peroxide; Manganese(II) chloride; Montmorillonite K10

Indexed keywords

EID: 77955843807     PISSN: 10018417     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cclet.2010.05.031     Document Type: Article

References (34)

1. Kockritz A., Sebek M., Dittmar A., et al. J. Mol. Catal. A 2006, 246:85.
2. Zhang S., Xu L., Trudell M.L. Synthesis 2005, 11:1757.
3. Heravi M.M., Ajami D., Aghapoor K., et al. Chem. Commun. 1999, 833.
4. Zhan B.Z., White M.A., Sham T.K., et al. J. Am. Chem. Soc. 2003, 125:2195.
5. Moorthy J.N., Singhal N., Venkatakrishnan P. Tetrahedron Lett. 2004, 45:5419.
6. Wolfson A., Wuyts S., De Vos D.E., et al. Tetrahedron Lett. 2002, 43:8107.
7. Loua J.D., Xu Z.N. Tetrahedron Lett. 2002, 43:8843.
8. Xu L., Trudell M.L. Tetrahedron Lett. 2003, 44:2553.
9. Lou J.D., Wang M., Zhu L.Y., et al. Catal. Commun. 2003, 4:647.
10. Reddy S.R., Das S., Punniyamurthy T. Tetrahedron Lett. 2004, 45:3561.
11. Heravi M.M., Derikvand F., Ghassemzadeh M., et al. Tetrahedron Lett. 2005, 46:6243.
12. Heravi M.M., Oskooie H.A., Kazemian P., et al. Phosphorus Sulfur Silicon 2004, 179:2341.
13. Heravi M.M., Farhangi N., Beheshtiha Y.S., et al. Indian J. Chem. Sect. B 2004, 43:430.
14. Heravi M.M., Sangsefidi L., Oskooie H.A., et al. Phosphorus Sulfur Silicon 2003, 178:707.
15. Tajbakhsh M., Ghaemi M., Sarabi S., et al. Monatsh. Chem. 2000, 131:1213.
16. Kaczorowska K., Kolarska Z., Mitka K., et al. Tetrahedron 2005, 61:8315.
17. Jones C.W. Applications of Hydrogen Peroxide and Derivatives 1999, Royal Soc. of Chem., Cambridge.
18. Anastas P.T., Warner J.C. Green Chemistry: Theory and Practice 1998, Oxford University Press, Oxford.
19. Anastas P.T., Heine L.G., Williamson T.C. Green Chem. Syn. & Proc. 2001, ACS, Ohio.
20. Tundo P., Anastas P., Black D.S., et al. Pure Appl. Chem. 2000, 72:1207.
21. Noyori R., Aoki M., Sato K. Chem. Commun. 2003, 1977.
22. Narayanan N., Bala Subramanian T.R. J. Chem. Res. Synop. 1992, 4:132.
23. Li D., Shi F., Guo Sh., et al. Tetrahedron Lett. 2004, 45:265.
24. Tamami B., Yaganeh H. React. Funct. Polym. 2002, 50:101.
25. Ezabadi A., Najafi Gh.R., Hashemi M.M. Chin. Chem. Lett. 2008, 19:1277.
26. Ezabadi A., Najafi Gh.R., Hashemi M.M. Chin. Chem. Lett. 2007, 18:1451.
27. Hashemi M.M., Ezabadi A., Karimi-Jaberi Z. Lett. Org. Chem. 2005, 2:559.
28. Hashemi M.M., Ghazanfari D., Ahmadibeni Y., et al. Synth. Commun. 2005, 35:1103.
29. Hashemi M.M., Karimi-Jaberi Z. Monatsh. Chem. 2004, 135:41.
30. Hashemi M.M., Karimi-Jaberi Z., Ghazanfari D. J. Chem. Res. 2004, 365.
31. Hashemi M.M., Khalili B., Eftekhari-Sis B. J. Chem. Res. 2005, 484.
32. Hashemi M.M., Akhbari M., Kaimi-jaberi Z. Lett. Org. Chem. 2006, 3:39.
33. Hashemi M.M., Kalantari F. Synth. Commun. 2000, 30:1857.
34. 1H NMR (300MHz, CDCl3) for selected compounds, Benzaldehyde: 9.8 (s, 1H), 7.4-7.8 (m, 5H), 4-methoxy-benzaldehyde: 9.9 (s, 1H), 7.8 (d, 2H, J=8.4Hz), 7.0 (d, 2H, J=8.4Hz), 3.9 (s, 3H). Acetophenone: 7.8-8.0 (m, 2H), 7.3-7.6 (m, 3H). Benzyl: 7.8-8.0 (m, 4H), 7.6-7.7 (m, 2H), 7.3-7.5 (m, 4H).