Green approaches to highly selective processes: Reactions of dimethyl carbonate over both zeolites and base catalysts

Pure and Applied Chemistry

Volumn 79, Issue 11, 2007, Pages 1855-1867

  Selva, Maurizio ^a  

^a CA' FOSCARI UNIVERSITY OF VENICE   (Italy)

Author keywords

Base catalysts; Dimethyl carbonate; Faujasite catalysts; Methylation reaction; Organic synthesis

Indexed keywords

EID: 36048952803     PISSN: 00334545     EISSN: None     Source Type: Journal    
DOI: 10.1351/pac200779111855     Document Type: Conference Paper

References (50)

1. (a) A.-A. G. Shaik, S. Sivaram. Chem. Rev. 96, 951 (1996);
2. (b) P. Tundo, M. Selva. Acc. Chem. Res. 35, 706 (2002).
3. (a) J. P. Senet. In The Recent Advance in Phosgene Chemistry, SNPE Group, France (1997);
4. (b) H. J. Buysch, H. Krimm, S. Boehm. U.S. patent 4335051, issued 15 June 1982, Bayer AG.
5. M. Massi Mauri, U. Romano, R. Tesei, P. Rebora. Ind. Eng. Chem. Prod. Res. Dev. 19, 396 (1980).
6. U. Romano, F. Rivetti, N. Di Muzio. U.S. patent 4318862, issued 9 March 1982, Anic SpA.
7. T. Matsuzaki, A. Nakamura. Catal. Surv. Jpn. 1, 77 (1997).
8. B. M. Bhanage, S.-I. Fujita, Y. Ikushina, M. Arai. Appl. Catal., A 219, 259 (2001).
9. (a) J. Haggin. Chem. Eng. News 70 (18), 25 (1992);
10. (b) M. A. Pacheco, C. L. Marshall. Energy Fuels 11, 2 (1997).
11. H. Cui, T. Wang, F. Wang, C. Gu, P. Wang, Y. Dai. Ind. Eng. Chem. Res. 42, 3865 (2003).
12. F. Rivetti, U. Romano, D. Delledonne. In Green Chemistry: Designing Chemistry for the Environment, P. Anastas, T. C. Williamson (Eds.), pp 70-80, ACS Symposium Series 626, American Chemical Society, Washington, DC (1996).
13. P. Tundo. In Continuous Flow Methods in Organic Synthesis, Horwood, Chichester (1991).
14. (a) E. K. Fukuoka, R. T. J. McIver. J. Am. Chem. Soc. 101, 2498 (1979);
15. (b) K. Takashima, S. M. Jose, A. T. do Amaral, J. M. Riveros. J. Chem. Soc., Chem. Commun. 1255 (1983).
16. (a) B. Trost. Science 254, 1471 (1991);
17. (b) A. Curzons, D. J. Constable, D. N. Mortimer, V. L. Cunnigham. Green Chem. 3, 1 (2001).
18. th ed., pp. 468-473, Wiley Interscience, New York (1992).
19. rd ed., Cambridge University Press, Cambridge (1989).
20. M. Mikolajczyk, S. Grzejszczak, A. Zatorski, F. Montanari, M. Cinquini. Tetrahedron Lett. 16, 3757 (1975).
21. M. Selva, C. A. Marques, P. Tundo. J. Chem. Soc., Perkin Trans. 1 1323 (1994).
22. (a) A. Bomben, C. A. Marques, M. Selva, P. Tundo. Tetrahedron 51, 11573 (1995);
23. (b) A. Bomben, M. Selva, P. Tundo. J. Chem. Res. (S) 448 (1997).
24. (a) P. Loosen, P. Tundo, M. Selva. U.S. patent 5278333, issued 1 November 1994, Tessenderloo Chemie;
25. (b) M. Selva, P. Tundo. CHEMTECH 25, 31 (1995).
26. (a) P. Tundo, M. Selva, A. Bomben. Org. Synth. 76, 169 (1999);
27. (b) A. Biasutti, M. Pierobon, M. Selva, P. Tundo. Unpublished results.
28. M. Selva, P. Tundo, A. Perosa, S. Memoli. J. Org. Chem. 67, 1071 (2002).
29. th ed., p. 411, Wiley Interscience, New York (1992).
30. F. Trotta, P. Tundo, G. Moraglio. J. Org. Chem. 52, 1300 (1987).
31. F. Schwochow, L. Puppe. Angew. Chem., Int. Ed. 14, 620 (1975).
32. (a) Z.-H. Fu Y. Ono. CaTTech. 1, 31 (1997);
33. (b) M. Selva, A. Bomben, P. Tundo. J. Chem. Soc., Perkin Trans. 1 1041 (1997).
34. (a) W.-C. Shieh, S. Dell, O. Repic. Org. Lett. 3, 4279 (2001);
35. (b) W.-C. Shieh, S. Dell, O. Repic. J. Org. Chem. 67, 2188 (2002);
36. (c) A. Perosa, M. Selva, P. Tundo, F. Zordan. Synlett 1, 272 (2000).
37. A. Ben Taleb, G. Jenner. J. Mol. Catal. L131-L136, 84 (1993).
38. (a) M. Selva, P. Tundo. EP Appl. 03029005.0, issued 16 December 2003, INCA Consortium;
39. (b) M. Selva, P. Tundo, A. Perosa. J. Org. Chem. 68, 7374 (2003).
40. (a) M. Selva. Synthesis 18, 2872 (2003);
41. (b) Y. Fu, T. Baba, Y. Ono. J. Catal. 197, 91 (2001).
42. M. Selva, P. Tundo, T. Foccardi. J. Org. Chem. 70, 2476 (2005).
43. M. Czjiek, T. Vogt, H. Fuess. Zeolites 11, 832 (1991).
44. (a) T. Beutel. J. Chem. Soc., Paradox Trans. 94, 985 (1998);
45. (b) F. Bonino, A. Damin, S. Bordiga, M. Selva, P. Tundo, A. Zecchina. Angew. Chem., Int. Ed. 44, 4774 (2005).
46. 3 bonds (which would be of a great diagnostic utility) cannot be observed because they fall within the zeolite framework region.
47. D. Barthomeuf. J. Phys. Chem. 88, 42 (1984).
48. M. Onaka, K. Ishikawa, Y. Izumi. Chem. Lett. 11, 1783 (1982).
49. M. Selva, P. Tundo, A. Perosa. J. Org. Chem. 67, 9238 (2002).
50. th ed., pp. 367-368, Wiley Interscience, New York (1992).