Remarkable acceleration on the transesterification reaction of 2-hydroxypropyl-p-nitrophenyl phosphate by ionic liquids

Catalysis Communications

Volumn 8, Issue 9, 2007, Pages 1383-1385

  Domingos, Josiel B ^a,b   Dupont, Jairton ^b  

^a FEDERAL UNIVERSITY OF SANTA CATARINA   (Brazil)

^b FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

Author keywords

Catalysis; HPNPP; Ionic liquids; Transesterification

Indexed keywords

IMIDAZOLIUM; METHYLIMIDAZOLIUM TETRAFLUOROBORATE; TRANSESTERIFICATION;

AROMATIC COMPOUNDS; CATALYSIS; ESTERIFICATION; REACTION RATES; WATER;

IONIC LIQUIDS;

EID: 34447574699     PISSN: 15667367     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.catcom.2006.12.007     Document Type: Article

References (24)

1. Anderson V.E., Ruszczycky M.W., and Harris M.E. Chem. Rev. 106 (2006) 3236-3251
2. Suh J., and Hong S.H. J. Am. Chem. Soc. 120 (1998) 12545
3. Liu S., and Hamilton A.D. Bioorg. Med. Chem. Lett. 7 (1997) 1779
4. Iranzo O., Kovalevsky A.Y., Morrow J.R., and Richard J.P. J. Am. Chem. Soc. 125 (2003) 1988
5. Manea F., Bodar Houillon F., Pasquato L., and Scrimin P. Angew. Chem. Int. Ed. Engl. 43 (2005) 6165
6. Molenveld P., Stikvoort W.M.G., Kooijman H., Speck A.L., Engbersen J.F.J., and Reinhoudt D.N. J. Org. Chem. 64 (1999) 3896
7. Hong I.S., and Suh J. Org. Lett. 2 (2000) 377-380
8. Dupont J., and Suarez P.A.Z. Phys. Chem. Chem. Phys. 8 (2006) 2441-2452
9. Wasserscheid P., and Keim W. Angew. Chem. Int. Ed. 39 (2000) 3773-3789
10. Welton T. Coord. Chem. Rev. 248 (2004) 2459-2477
11. Consorti C.S., Suarez P.A.Z., de Souza R.F., Burrow R.A., Farrar D.H., Lough A.J., Loh W., da Silva L.H.M., and Dupont J. J. Phys. Chem. B 109 (2005) 4341-4349
12. Gozzo F.C., Santos L.S., Augusti R., Consorti C.S., Dupont J., and Eberlin M.N. Chem.-Eur. J. 10 (2004) 6187-6193
13. Dupont J., and Braz J. Chem. Soc. 15 (2004) 341-350
14. Schroder U., Wadhawan J.D., Compton R.G., Marken F., Suarez P.A.Z., Consorti C.S., de Souza R.F., and Dupont J. New J. Chem. 24 (2000) 1009-1015
15. Wadhawan J.D., Schroder U., Neudeck A., Wilkins S.J., Compton R.G., Marken F., Consorti C.S., de Souza R.F., and Dupont J. J. Electroanal. Chem. 493 (2000) 75-83
16. De Diego T., Lozano P., Gmouh S., Vaultier M., and Iborra J.L. Biomacromolecules 6 (2005) 1457-1464
17. Antonietti M., Kuang D.B., Smarsly B., and Yong Z. Angew. Chem. Int. Ed. 43 (2004) 4988-4992
18. Bunton C.A., and Farber S.J. J. Org. Chem. 34 (1969) 767-772
19. Kirby A.J., and Younas M. J. Chem. Soc. B (1970) 510-513
20. 1H NMR spectrum, as observed with the authentic material, the UV-vis absorption spectra support that PNP is major present at the end of the reaction as its protonated form.
21. Sievers C., Jimenez O., Muller T.E., Steuernagel S., and Lercher J.A. J. Am. Chem. Soc. 128 (2006) asap
22. Dupont J., and Spencer J. Angew. Chem. Int. Ed. 43 (2004) 5296-5297
23. Cassol C.C., Ebeling G., Ferrera B., and Dupont J. Adv. Synth. Catal. 348 (2006) 243-248
24. Brown D.M., and Usher D.A. J. Chem. Soc. (1965) 6558-6564