An environment-friendly method for synthesis of 1,4-dibromo-naphthalene in aqueous solution of ionic liquids

Catalysis Communications

Volumn 9, Issue 13, 2008, Pages 2179-2182

  Zhao, Xinhua ^a   Gu, Yingying ^a   Li, Jiang ^a   Ding, Hanming ^a   Shan, Yongkui ^a  

^a EAST CHINA NORMAL UNIVERSITY   (China)

Author keywords

1,4 Dibromonaphthalene; Bromination; Ionic liquids; Naphthalene

Indexed keywords

BROMINE; CATALYSIS; FLUIDS; IONIZATION OF LIQUIDS; LIQUIDS; NAPHTHALENE; POLYCYCLIC AROMATIC HYDROCARBONS; SOLUTIONS;

(E ,3E) PROCESS; AQUEOUS SOLUTIONS; BROMINE ATOMS; DIALKYLIMIDAZOLIUM; ELSEVIER (CO); ENVIRONMENT FRIENDLY; PYRIDINIUM; SYNTHESIS (OF CHIRAL IONIC LIQUIDS);

IONIC LIQUIDS;

EID: 46449098496     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2008.04.020     Document Type: Article

References (35)

1. Osman C., Ismail K., Ibrahim D., Tuncer H., and Keith S. Collect. Czech. Chem. Commun. 65 (2000) 1791
2. Krock F.W., and Neeff R. Eur. Chem. Abstr. 97 (1982) 144615
3. Bacon B.G.R., and Stewart O. J. Chem. Soc. 49 (1965) 53
4. Cakmak O., Demirtas I., and Balaydin H.T. Tetrahedron 58 (2002) 5603
5. Qinglan H., Evmenenko G.A., Dutta P., Lee P., Armstrong N.R., and Marks T.J. J. Am. Chem. Soc. 127 (2005) 10227
6. Lambert C., Risko C., Coropceanu V., Schelter J., Amthor S., Gruhn N., Durivage J., and Bredas J.L. J. Am. Chem. Soc. 127 (2005) 8508
7. Dastan A., Tahir M.N., Ülkü D., and Balci M. Tetrahedron 55 (1999) 12853
8. Yanovskaya L.A. Dokl. Akad. Nauk SSSR 17 (1950) 693
9. Terent'ev A.P., Belen'kii L.I., and Yanovskaya L.A. Zhur. Obshchei. Khim. 24 (1954) 1265
10. Bayer R.W., and O'Reilly E.J. J. Org. Chem. 23 (1958) 311
11. Kodomari M., Satoh H., and Yoshitomi S. J. Org. Chem. 53 (1988) 2093
12. Sheldon R., and Gallopoulos N. Sci. Am. 261 (1989) 94
13. Wasserscheid P., and Keim W. Angew. Chem. Int. Edit. 39 (2000) 3772
14. Bonhôte P., Dias A., Papageorgiou N., Kalyanasundaram K., and Gra1tzel M. Inorg. Chem. 35 (1996) 1168
15. Chiappe C., Leandri E., and Pieraccini D. Chem. Commun. 22 (2004) 2536
16. Breslow R. Acc. Chem. Res. 24 (1991) 159
17. Li C.J. Chem. Rev. 93 (1993) 2023
18. Gu Y., Ogawa C., Kobayashi J., Mori Y., and Kobayashi S. Angew. Chem. Int. Edit. 45 (2006) 7217
19. Chen L., and Li C. Adv. Synth. Catal. 348 (2006) 1459
20. Welton T. Chem. Rev. 99 (1999) 2071
21. Wasserscheid P., and Keim W. Angew. Chem. Int. Edit. 39 (2000) 3772
22. Wilkes J.S. Green Chem. 4 (2002) 73
23. Zerth H.M., Leonard N.M., and Mohan R.S. Org. Lett. 5 (2003) 55
24. Kumar A., and Pawar S.S. J. Org. Chem. 69 (2004) 1419
25. Chiappe C., Capraro D., Conte V., and Pieraccini D. Org. Lett. 3 (2001) 1061
26. Chan L.J., and Jung P.H. Synthetic Commun. 37 (2007) 87
27. Pârvulescu V., and Hardacre C. Chem. Rev. 107 (2007) 2615
28. Sun W., Xia C.G., and Wang H.W. Tetrahedron Lett. 44 (2003) 2409
29. Akaiyama T., Suzuki A., and Fuchibe K. Synlett 6 (2005) 1024
30. Rajagopal R., Jarikote D.V., Lahoti R.J., Daniel T., and Srinivasan K.V. Tetrahedron Lett. 44 (2003) 1815
31. Lee K.M., Lee C.K., and Lin I.J.B. Chem. Commun. 9 (1997) 899
32. Barhate N.B., Gajare A.S., Wakharkar R.D., and Bedekar A.V. Tetrahedron 55 (1999) 11127
33. Furia V.C.F.D., and Moro S. Tetrahedron Lett. 35 (1994) 7429
34. Clague M.J., and Butler A. J. Am. Chem. Soc. 117 (1995) 3415
35. Choudary B.M., Sudha Y., and Reddy P.N. Synlett 6 (1994) 450