Efficient synthesis of benzophenone derivatives in Lewis acid ionic liquids

Catalysis Communications

Volumn 8, Issue 11, 2007, Pages 1834-1837

  Li, Changzhi ^a,b   Liu, Wujun ^a,b  

^a Kent)   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Acylation; Benzophenone; Friedel Crafts reaction; Ionic liquids; Lewis acid

Indexed keywords

ACYLATION; CATALYST ACTIVITY; DERIVATIVES; FRIEDEL-CRAFTS REACTION; IONIC LIQUIDS; ORGANIC SOLVENTS; REACTION RATES;

BENZOPHENONE; LEWIS ACID; REACTION SYSTEMS;

BENZENE;

EID: 34548701110     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2007.02.023     Document Type: Article

References (34)

1. Olah G.A. Friedel-Crafts and Related Reaction vol. III (1964), Interscience, New York Part I
2. Szmant H. Organic Building Blocks of the Chemical Industry (1989), Wiley, New York
3. March J. Advanced Organic Chemistry. fourth ed. (1992), Wiley, New York
4. Bohm M., Mitsch A., Wissner P., Sattler I., and Schlitzer M. J. Med. Chem. 44 (2001) 3117
5. Chan J.H., Freeman G.A., Tidwell J.H., Romines K.R., Schaller L.T., Cowan J.R., Gonzales S.S., Lowell G.S., Andrews C.W., Reynolds D.J., St Clair M., Hazen R.J., Ferris R.G., Creech K.L., Roberts G.B., Short S.A., Weaver K., Koszalka G.W., and Boone L.R. J. Med. Chem. 47 (2004) 1175
6. Husain S.S., Nirthanan S., Ruesch D., Solt K., Cheng Q., Li G.D., Arevalo E., Olsen R.W., Raines D.E., Forman S.A., Cohen J.B., and Miller K.W. J. Med. Chem. 49 (2006) 4818
7. For a review, see. Bagheri H., Lhiaubet V., Montastruc J.L., and Chouini-Lalanne N. Drug. Saf. 22 (2000) 339
8. Nishimura G., Ishizumi K., Shiraishi Y., and Hirai T. J. Phys. Chem. B 110 (2006) 21596
9. Ferreira L.F.V., Machado I.F., Da Silva J.P., and Branco T.J.F. Photochem. Photobiol. Sci. 5 (2006) 665
10. Prucker O., Naumann C.A., Ruhe J., Knoll W., and Frank C.W. J. Am. Chem. Soc. 121 (1999) 8766
11. Wang H.Y., Wei J., Jiang X.S., and Yin J. J. Polym. Sci. Polym. Chem. 44 (2006) 3738
12. Karrer F., Meier H., and Pascual A. J. Fluorine Chem. 103 (2000) 81
13. Jia C.G., Huang M.Y., and Jiang Y.Y. Chin. J. Chem. 5 (1993) 452
14. Kowalski K., Zakrzewski J., and Jerzykiewicz L. J. Organomet. Chem. 690 (2005) 1474
15. Wine G., Pham-Huu C., and Ledoux M. Catal. Commun. 7 (2006) 768
16. Patil P.T., Malshe K.M., Kumar P., Dongare M.K., and Kemnitz E. Catal. Commun. 3 (2002) 411
17. Laidlaw P., Bethell D., Brown S.M., and Hutchings G.J. J. Mol. Catal. A 174 (2001) 187
18. Zhou D.Q., Zhang Y.H., Huang M.Y., and Jiang Y.Y. Polym. Adv. Technol. 14 (2003) 360
19. Choudary B.M., Rao B.P.C., Chowdari N.S., and Kantam M.L. Catal. Commun. 3 (2002) 363
20. Choudhary V.R., Jana S.K., and Patil N.S. Tetrahedron Lett. 43 (2002) 1105
21. Evans D.A., Fandrick K.R., and Song H.J. J. Am. Chem. Soc. 127 (2005) 8942
22. Yin D.H., Li C.Z., Tao L., Yu N., Hu S., and Yin D.L. J. Mol. Catal. A 245 (2006) 260
23. Yin D.H., Li C.Z., Li B.M., Tao L., and Yin D.L. Adv. Synth. Catal. 347 (2005) 137
24. Huddleston J.G., Willauer H.D., Swatloski R.P., Visser A.E., and Rogers R.D. Chem. Commun. (1998) 1765
25. Gutowski K.E., Broker G.A., Willauer H.D., Huddleston J.G., Swatloski R.P., Holbrey J.D., and Rogers R.D. J. Am. Chem. Soc. 125 (2003) 6632
26. Yang Y.L., and Kou Y. Chem. Commun. (2004) 226
27. Choudhary V.R., Jana S.K., and Patil N.S. Catal. Lett. 76 (2001) 235
28. Corma A., and García H. Chem. Rev. 103 (2003) 4307
29. Csihony S., Mehdi H., and Horváth I.T. Green Chem. 3 (2001) 307
30. Frost C.G., Hartley J.P., and Griffin D. Tetrahedron Lett. 43 (2002) 4789
31. Piao L.Y., Fu X., Yang Y.L., Tao G.H., and Kou Y. Catal. Today 93-95 (2004) 301
32. Xiao Y., and Malhotra S.V. J. Mol. Catal. A 230 (2005) 129
33. Xiao Y., and Malhotra S.V. J. Organomet. Chem. 690 (2005) 3609
34. Earle M.J., Hakala U., Hardacre C., Karkkainen J., McAuley B.J., Rooney D.W., Seddon K.R., Thompson J.M., and Wähälä K. Chem. Commun. (2005) 903