Green preparation of quinoline derivatives through FeCl3· 6H2O Friedlander reaction in ionic liquids

Canadian Journal of Chemistry

Volumn 82, Issue 7, 2004, Pages 1192-1196

  Wang, Jianji ^a   Fan, Xuesen ^a   Zhang, Xinying ^a   Han, Lijun ^a  

^a HENAN NORMAL UNIVERSITY   (China)

Author keywords

Friedlander reaction; Green chemistry; Ionic liquid; Quinoline derivatives

Indexed keywords

CATALYSTS; CONDENSATION; DERIVATIVES; IRON COMPOUNDS; REACTION KINETICS;

IRON CHLORIDE; QUINOLINES; REACTION MEDIUM;

NITROGEN COMPOUNDS;

FERROUS CHLORIDE; QUINOLINE DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL REACTION; REACTION ANALYSIS; SYNTHESIS;

EID: 10644236353     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/v04-066     Document Type: Article

References (23)

1. (a) A.R. Katritzky and C.N. Rees. In Comprehensive heterocyclic chemistry. Edited by A.J. Boulton and A. McKillop. Vol. 2. Pergamon Press, Oxford. 1984;
2. (b) T.L. Gilchist. Heterocyclic chemistry. Longmans, London. 1997.
3. (a) G. Jones. In Comprehensive heterocyclic chemistry. Edited by A.R. Katritzky, C.W. Rees, and R.F.V. Scriven. Vol. 5. Pergamon Press, Oxford. 1996. Chap. 5.05. p. 167;
4. (b) H. Tokuyama, M. Sato, T. Ueda, and T. Fukuyama. Heterocycles, 54, 105 (2001);
5. (c) N.J. Ton and E.M. Ruel. Synthesis, 1351 (2001).
6. (a) P. Friedlander. Ber. 15, 2572 (1882);
7. (b) R.C. Elderfield. In The chemistry of heterocyclic compounds. Edited by R.C. Elderfield. Vol. 4. John Wiley & Sons, New York. 1952.
8. E.A. Fehnel. J. Org. Chem. 31, 2899 (1966).
9. (a) J. Dupont, R.F. de Souza, and P.A.Z. Suarez. Chem. Rev. 102, 3667 (2002);
10. (b) D.B. Zhao, M. Wu, Y. Kou, and E.Z. Min. Catal. Today, 74, 157 (2002);
11. (c) H. Olivier-Bourbigou and L. Magna. J. Mol. Catal. A, 182-183, 419 (2002);
12. (d) T. Welton. Chem. Rev. 99, 2071 (1999);
13. (e) Z. Li and C.G. Xia. Tetrahedron Lett. 44, 2069 (2003);
14. (f) J.S. Yadav, B.V.B. Reddy, A.K. Basak, and A. Venkat Narsaiah. Tetrahedron Lett. 44, 1047 (2003).
15. (a) X. Zhang, H. Niu, and J. Wang. J. Chem. Res. (S) 33 (2003);
16. (b) X. Zhang, X. Fan, H. Niu, and J. Wang. Green Chem. 5, 267 (2003).
17. (a) J. Christoffers. J. Chem. Soc., Perkin Trans, 1, 3141 (1997);
18. (b) J. Lu, H.R. Ma, and W.H. Li. Chin. J. Org. Chem. 20, 815 (2000).
19. J.D. Holbrey and K.R. Seddon. J. Chem. Soc., Dalton Trans. 2133 (1999).
20. R. Leardini, D. Nanni, A. Tundo, G. Zanardi, and F. Ruggieri. J. Org. Chem. 57, 1842 (1992).
21. M. Al-Talib, J.C. Jochims, Q. Wang, A. Hamed, and A.E. Ismail. Synthesis, 875 (1992).
22. Y. Toi, K. Isagawa, Y. Fushizaki. Nippon Kagaku Zasshi, 89, 1096 (1968); Chem. Abstr. 70, 87508 (1969).
23. Y. Toi, K. Isagawa, Y. Fushizaki. Nippon Kagaku Zasshi, 89, 1096 (1968); Chem. Abstr. 70, 87508 (1969).