Catalysis in the production and reactions of dimethyl carbonate, an environmentally benign building block

Applied Catalysis A: General

Volumn 155, Issue 2, 1997, Pages 133-166

  Ono, Yoshio ^a  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

Dimethyl carbonate; Diphenyl carbonate; Isocyanate; Methoxycarbonylation; Methylation; Tetramethoxysilane; Transesterification

Indexed keywords

EID: 30244508498     PISSN: 0926860X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0926-860X(96)00402-4     Document Type: Review

References (75)

1. A.S, Gorden and W.P. Norris, J. Phys. Chem., 69 (1965) 3013.
2. P. Tundo and M. Selva, ChemTech, 25(5) (1995) 31.
3. L. Cassar, Chim. Ind., 72 (1990) 18.
4. U. Romano, Chim. Ind., 75 (1993) 303.
5. N. Rivettti and U. Romano, J. Organometal. Chem., 174 (1979) 221.
6. D. Delledonne, F. Rivetti and U. Romano, J. Organometal. Chem., 488 (1995) C15.
7. F. Rivetti, U. Romano, D. Delledonne, in: P.T. Anastsa, T.C. Williamson (Eds.), ACS Symposium Ser. No. 626, Green Chemistry, Designing Chemistry for the Environment, American Chemical Society, Washington, 1996, p. 70.
8. U. Romano, R. Tesei, MM. Marui and P. Rebora, Ind. Eng. Chem., Prod. Res. Dev., 19 ( 1980) 396.
9. Chem. Eng. News 65 (1987) (39) 26.
10. K. Nishihira, N. Matsuzaki and S. Tanaka, Shokubai, 37 (1995) 68.
11. Chem. Eng. News, 4 May (1992) 25.
12. J.F. Knifton and R.G. Duranleau, J. Mol. Catal., 67 (1991) 380.
13. P. Tundo, G. Moraglio and F. Trotta, Ind. Eng. Chem. Res., 28 (1989) 881.
14. P. Tundo, F. Trotta and G. Moraglio, J. Chem. Soc., Perkin Trans., 1 (1989) 1070.
15. M. Makozka, Tetrahedron, 24 (1968) 175.
16. M. Makozka, Pure and Appl. Chem., 43 (1975) 439.
17. M. Mikolajcznik, S. Grzejszczak, A. Zatorski, F. Montanari and M. Cinquiy, Tetrahedron Lett., (1975) 3757.
18. M. Selva, A. Marques and P. Tundo, J. Chem. Soc., Perkin Trans., 1 (1994) 1323.
19. P. Tundo, M. Selva, C.A. Marques, in: P.T. Anastsa, T.C. Williamson (Eds.), ACS Symposium Ser. No. 626, Green Chemistry, Designing Chemistry for the Environment, American Chemical Society, Washington, 1996, p. 81.
20. Z.-H. Fu and Y. Ono, J. Catal., 145 (1994) 166.
21. A.B. Taleb and C. Jenner, J. Mol. Catal., 84 (1993) L121.
22. M. Lissel, S. Schmidt and B. Neumann, Synthesis, (1986) 382,
23. P. Tundo, F. Trotta, G. Moraglio and F. Ligorati, Ind. Eng. Chem. Res., 27 (1988) 1565.
24. M.S. Newman and J.A. Cella, J. Org. Chem., 39 (1974) 214.
25. G. Iori, U. Romano, UK Patent Appl. GB 2026484 (1980).
26. Z.-H. Fu and Y. Ono, Catal. Lett., 21 (1993) 41.
27. R.F. Parton, J.M. Jacobs, D.R. Huybrechts and P.A. Jacobs, Stud. Surf Sci. Catal., 46 (1989) 163.
28. M.M. Mauri, U. Romano and F. Rivetti, Ing. Chim. Ital., 21 (1985) 6.
29. Y. Ono, Y. Fu, T. Baba, to be submitted.
30. S. Porche, S. Su, R. Doepper and R. Rinnken, Chem. Ing. Tech., 65 (1993) 203.
31. Y. Tamura, T. Saito, H. Ishibashi and M. Ikeda, Synthesis, (1975) 641.
32. F. Trotta, P. Tundo and G. Morsglio, J. Org. Chem., 52 (1987) 1300.
33. Z.-H. Fu, Y. Ono, Catal. Lett. 22 (1993) 277; 18 (1993) 59.
34. Z.-H. Fu, Y. Ono, Catal. Lett. 22 (1993) 277; 18 (1993) 59.
35. P.R.P. Rao, P. Massiani and D. Barthomeuf, Catal. Lett., 31 (1995) 115.
36. Y.H. Evance and A.N. Brown, Can. J. Chem., 29 (1951) 1.
37. A.G. Hill, J.H. Shipp and A.J. Hill, Ind. Eng. Chem., 43 (1951) 1579.
38. N. Takamiya, K. Koinuma, K. Ando and S. Murai, Nihon Kagaku Kaishi, (1979) 1453.
39. D.Y. Chen, M.C. Chu, N.S. Chung and XK. Chuang, Stud. Surf. Sci. Catal., 28 (1986) 739.
40. M. Lissel, Liebigs Ann. Chem., (1987) 77.
41. H. Jansen in der War and M. Lissel, Z. Naturforsch., 44b (1989) 863.
42. H. Jansen in der War and M. Lissel, Z. Chem., 29 (1989) 253.
43. M. Lissel and A.R. Rohani-Dezfuli, Chem. Ztg., 111 (1987) 83.
44. US Patent 5206408.
45. Eur. Patent Appl. 89709.
46. Chem. Brit. 12 (1994) 970.
47. K. Komiya, S. Fukuoka, M. Aniinaka, K. Hasegawa, H. Hachiya, H. Okamoto, T. Watanabe, H. Yoneda, T. Dozono, in: P.T. Anastsa, T.C. Williamson (Eds.), ACS Symposium Ser. No. 626, Green Chemistry, Designing Chemistry for the Environment, American Chemical Society, Washington, 1996, p. 20.
48. A-A.G. Shaikh and S. Sivaram, Ind. Eng. Chem. Res., 31 (1992) 1167.
49. US Patent 358 493, 565 895, 565 896; Japan Kokai, 87-277 345, 92-7035, 93-123579.
50. Japan Kokai, 67-105 032, 92-7035.
51. Japan Kokai, 67-105032.
52. Japan Kokai, 82-183745.
53. Japan Kokai, 82-176932.
54. Japan Kokai, 91-200 746, 91-236 354.
55. Japan Kokai, 79-125 617.
56. Japan Kokai, 82-176 932, 89-93 560, 92-9358.
57. US Patent 404 556.
58. Z.-H. Fu, Y. Ono, J. Mol. Catal., in press.
59. L. Ruest, C. Blouin and P. Deslongchamps, Syn. Commun., 6 (1976) 169.
60. M.L. Quesada and E.H. Schlessinger, J. Org. Chem., 43 (1978) 346.
61. R.M. Sandifer, A.K. Bhattacharya and T.M. Harris, J. Org. Chem., 46 (1981) 2261.
62. S. Iwatsuki, T. Itoh and K. Nishihara, Chem. Lett., (1992) 517.
63. M. Selva, C.A. Marques and F. Tundo, Gazz. Chim. Ital., 123 (1993) 515.
64. F. Porta, S. Cenni, M. Pizzott and C. Crotti, Gazz. Chim. Ital., 115 (1985) 275.
65. M. Lissel, A.R. Rohani-Dezfuni, G. Vogt, J. Chem. Research (S) (1989) 312; (M) (1989) 2434.
66. M. Lissel, A.R. Rohani-Dezfuni, G. Vogt, J. Chem. Research (S) (1989) 312; (M) (1989) 2434.
67. Japan Kokai, 79-163 527, 80-4 316; US Patent 4 268 863, 4 268 864; EU Patent 48 371.
68. Z.-H. Fu and Y. Ono, J. Mol. Catal., 91 (1994) 399.
69. D. Sengupta, R. V. Venkateswaran, J. Chem. Research (S) (1984) 372.
70. C.A. Marques, M. Selva, P. Tundo and M. Montanari, J. Org. Chem., 58 (1993) 5765.
71. E. Suzuki, M. Akiyama and Y. Ono, J. Chem. Soc., Chem. Commun., (1992) 136.
72. Y. Ono, M. Akiyama and E. Suzuki, Chem. Mater., 5 (1993) 442.
73. T. Suzuki, E. Suzuki, Y. Ono, to be published.
74. M. Akiyama, E. Suzuki and Y. Ono, Inorg. Chim. Acta, 207 (1993) 259.
75. Y. Ono, A. Kusano, H. Hatayama, E. Suzuki, J. Mater. Chem., submitted for publication.