Efficient regioselective carboxylation of phenol to salicylic acid with supercritical CO2 in the presence of aluminium bromide

Journal of Molecular Catalysis A: Chemical

Volumn 295, Issue 1-2, 2008, Pages 52-56

  Iijima, Takayuki ^a   Yamaguchi, Tatsuaki ^a  

^a CHIBA INSTITUTE OF TECHNOLOGY   (Japan)

Author keywords

Carboxylation; Lewis acid; Phenol; Regioselective; Supercritical carbon dioxide

Indexed keywords

AROMATIC HYDROCARBONS; CARBON; CARBON DIOXIDE; CARBOXYLATION; CATALYSIS; CATALYSTS; OXIDES; PHENOLS; SILANES; SUPERCRITICAL FLUID EXTRACTION;

CHLOROTRIMETHYLSILANE; EFFICIENT; EXCELLENT YIELDS; LEWIS ACID; LEWIS ACID CATALYSTS; LEWIS ACIDS; MODERATE TEMPERATURES; OPTIMIZED CONDITIONS; REACTION CONDITIONS; REACTION MECHANISMS; REGIOSELECTIVE; REGIOSELECTIVE CARBOXYLATIONS; SALICYLIC ACIDS; SUPERCRITICAL CARBON DIOXIDE; SUPERCRITICAL CO;

ACIDS;

EID: 54049156388     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2008.07.017     Document Type: Article

References (26)

1. Bakker D., and Watson A. Nature 410 (2001) 765
2. Kyoto Protocol to the United Nations Framework Convention on Climate Change, 1997.
3. Cott D.J., Ziegler K.J., Owens V.P., Glennon J.D., Graham A.E., and Holtmes J.D. Green Chem. 7 (2005) 105
4. Hyde J.R., Walsh B., Singh J., and Poliakoff M. Green Chem. 7 (2005) 357
5. Jessop P.G., Ikariya T., and Noyori R. Science 269 (1995) 1065
6. Arakawa H., Areata M., Armor J.N., Barteau M.A., Beckman E.J., Bell A.T., Bercaw J.E., Creutz C., Dinjus E., Dixon D.A., Domen K., DuBois D.L., Eckert J., Fujita E., Gibson D.H., Goddard W.A., Goodman D.W., Keller J., Kubas G.J., Kung H.H., Manzer J.E., Marks T.J., Morokuma K., Nicholas K.M., Periana R., Que L., Rostrup-Nielson J., Sachtler W.M.H., Schmidt L.D., Sen A., Somorjai G.A., Stair P.C., Stults B.R., and Tumas W. Chem. Rev. 101 (2001) 953
7. Iijima T., Takagi D., and Yamaguchi T. J. Jpn. Petrol. Inst. 51 (2008) 65
8. Iijima T., and Yamaguchi T. Tetrahedron Lett. 48 (2007) 5309
9. Iijima T., Iwase T., and Yamaguchi T. J. Jpn. Petrol. Inst. 49 (2006) 206
10. Lindsey A.S., and Jeskey H. Chem. Rev. 57 (1957) 583
11. Sasson Y., and Razintsky M. J. Chem. Soc., Chem. Commun. (1985) 1134
12. Komiyama M., and Hirai H. J. Am. Chem. Soc. 106 (1984) 174
13. Iijima T., and Yamaguchi T. Appl. Catal. A: Gen. 345 (2008) 12
14. Suzuki Y., Hattori T., Okuzawa T., and Miyano S. Chem. Lett. 31 (2002) 102
15. Olah G.A., Torok B., Joschek J.P., Bucsi I., Esteves P.M., Rasul G., and Prakash G.K.S. J. Am. Chem. Soc. 124 (2002) 11379
16. Kajimoto O. Chem. Rev. 99 (1999) 355
17. Fujita S., Bhanage B.M., Ikushima Y., and Arai M. Green Chem. 3 (2001) 87
18. Sakakura T., Saito Y., Okano M., Choi J., and Sako C.T. J. Org. Chem. 63 (1998) 7095
19. Du Y., Cai F., Kong D.-L., and He L.-N. Green Chem. 7 (2005) 518
20. Gonzalez J.G., Molina M.J., Rodriguez F., and Mirada F. J. Chem. Eng. Date 46 (2001) 918
21. Gurdial G.S., and Foster N.R. Ind. Eng. Chem. Res. 30 (1991) 575
22. Dunn G.E., Janzen E.G., and Rodewald W. Can. J. Chem. 46 (1968) 2905
23. Nemoto K., Yoshida H., Suzuki Y., Morohashi N., and Hattori T. Chem. Lett. 35 (2006) 820
24. Zareyee D., and Karimi B. Tetrahedron Lett. 48 (2007) 1277
25. Naeimi H., and Moradi L. J. Mol. Catal. A 256 (2006) 242
26. Casiragi G., Casnati G., Cornia M., Pochini A., Puglia G., Saratori G., and Ungaro R. J. Chem. Soc., Perkin Trans. 1 (1978) 318