Oxidative carbonylation of methanol to dimethyl carbonate by chlorine-free homogeneous and immobilized 2,2′-bipyrimidine modified copper catalyst

Collection of Czechoslovak Chemical Communications

Volumn 72, Issue 8, 2007, Pages 1094-1106

  Csihony, Szilárd ^a   Mika, László T ^a   Vlád, Gábor ^a   Bárta, Katalin ^a   Mehnert, Christian P ^b   Horváth, István T ^a  

^a EÖTVÖS LORÁND UNIVERSITY   (Hungary)

^b EXXONMOBIL UPSTREAM RESEARCH COMPANY   (United States)

Author keywords

2,2 bipyrimidine; Copper; Dimethyl carbonate; Homogeneous catalysis; Immobilized catalysts; Methanol; Oxidative carbonylation

Indexed keywords

EID: 34948890564     PISSN: 00100765     EISSN: None     Source Type: Journal    
DOI: 10.1135/cccc20071094     Document Type: Article

References (37)

1. Tundo P., Selva M.: Ace Chem. Res. 2002, 35, 706.
2. Shaikh A.-A. G., Sivaram S.: Chem. Rev. 1996, 96, 951.
3. a) Abrams E. in: Encyclopedia of Chemical Technology (Kirk-Othmer), 3rd ed., Vol. IV, p. 758. Wiley, New York 1979, and references therein;
4. b) Cotarca L., Eckert H. in: Phosgenations - A Handbook. Wiley, Hoboken 2004.
5. a) Romano U., Tesei R., Mauri M. M., Rebora P.: Ind. Eng. Chem. Prod. Res. Dev. 1980, 19, 396;
6. b) Paret G., Donati G. Ghirardini M.: U.S, 5,536,864 (1996), Chem. Abstr. 1992, 116, 62046;
7. c) Rivetti F., Romano U.: Eur. 534,545, Chem. Abstr. 1993, 119, 138752.
8. Romano U., Rivetti F., Delledonne D.: J. Organomet. Chem. 1995, 488, C15.
9. a) Fenton D. M., Steinwald J.: J. Org. Chem. 1974, 39, 701;
10. b) Rivetti F., Romano U.: J. Organomet. Chem. 1978, 154, 323;
11. c) Rivetti F., Romano U.: J. Organomet. Chem. 1979, 174, 221;
12. d) Kondo K., Sonoda N., Tsutsumi S.: Tetrahedron Lett. 1971, 411.
13. a) Kizlink J., Pastucha I.: Collect. Czech. Chem. Commun. 1995, 60, 687;
14. b) Kizlink J., Pastucha I.: Collect. Czech. Chem. Commun. 1994, 59, 2116;
15. c) Aresta M., Dibenedetto A., Pastore C., Pápai I., Schubert G.: Top. Catal. 2006, 40, 71;
16. d) Sakakura T., Saito Y., Okano M., Choi J.-C., Sako T.: J. Org. Chem. 1998, 63, 7095;
17. e) Drake I. J., Fujdala K. L., Bell A. T., Tilley D. T.: J. Catal. 2005, 230, 14;
18. f) Zhang Y., Drake I. J., Briggs D. N., Bell A. T.: J. Catal. 2006, 244, 219;
19. g) Richter M., Fait M. J. G., Eckelt R., Schneider M., Radnik J., Heidemann D., Fricke R.: J. Catal. 2007, 245, 11.
20. Vlád G., Horváth I. T.: J. Org. Chem. 2002, 67, 6550.
21. Horváth I. T., Ponce E. C.: Rev. Sci. Instrum. 1991, 62, 1104.
22. Fried J., Elderfield R. C.: J. Org. Chem. 1941, 6, 577.
23. Kurek J. T., Vogel G. J.: J. Heterocycl. Chem. 1968, 5, 275.
24. Hermann K., Simchen G.: Liebigs Ann. Chem. 1981, 333.
25. Schaefer F., Peters A. G.: J. Org. Chem. 1961, 26, 412.
26. Kvita V.: Synthesis 1986, 786.
27. a) Periana R. A., Taube D. J., Gamble S., Taube H., SatohT., Fujii H.: Science 1998, 280, 560;
28. b) Bhattacharya A. K.: U.S. 4,761,467 (1988),
29. Chem. Abstr. 1987, 107, 22960.
30. 3OD: 48.07 sept.
31. a) Bruce M. I.: J. Organomet. Chem. 1972, 44, 209;
32. b) Pasquali M., Floriani C., Gaetani-Manfredotti A.: Inorg. Chem. 1981, 20, 3382.
33. Brubaker C. H., Wicholas M.: J. Inorg. Nucl. Chem. 1965, 27, 59.
34. a) Saegusa T., Tsuda T., Isayama K.: J. Org. Chem. 1970, 35, 2976;
35. b) Pasquali M., Floriani C., Gaetani-Manfredotti A.: Inorg. Chem. 1981, 20, 3382.
36. a) Raab V., Merz M., Sundermeyer J.: J. Mol. Catal. A: Chem. 2001, 175, 51;
37. b) Hu J.-C., Cao Y., Yang P., Deng J.-F., Fan K.-N.: J. Mol. Catal. A: Chem. 2002, 185, 1.