Hydrogenation of styrene oxide in the presence of supported platinum catalysts to produce 2-phenylethanol

Journal of Molecular Catalysis A: Chemical

Volumn 261, Issue 1, 2007, Pages 98-103

  Kirm, Ilham ^a   Medina, Franscisco ^a   Sueiras, Jesús E ^a   Salagre, Pilar ^a   Cesteros, Yolanda ^a  

^a UNIVERSITAT ROVIRA I VIRGILI   (Spain)

Author keywords

2 Phenylethanol; Platinum catalysts; Styrene oxide hydrogenation

Indexed keywords

ALCOHOLS; ALUMINA; CATALYSTS; HYDROGENATION; PLATINUM; X RAY DIFFRACTION ANALYSIS;

2-PHENYLETHANOL; PLATINUM CATALYSTS; STYRENE OXIDE HYDROGENATION;

STYRENE;

EID: 33845207993     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2006.07.043     Document Type: Article

References (56)

1. K. Bauer, D. Garbe, H. Surburg, Common Fragrance and Flavor Materials, VCH publishers, New York, 1990.
2. Theimer E.T. Theimer in Fragrance Chemistry (1982), Academic Press, New York p. 271
3. In: Mookherjee B.D., and Wilson R.A. (Eds). Kirk-Othmer Encyclopedia of Chemical Technology, vol. 4. fourth ed. (1996), John Wiley and Sons, New York
4. C.V. Rode, V.S. Kshirsagar, V.H. Rane, R.V. Chaudhari, US Patent 6,979,753 (2005).
5. Theimer T.E. Fragrance Chemistry (1982), Academic Press, New York p. 271
6. R.V. Chaudhari, M.M. Telkar, C.V. Rode, US Patent 6,166,269 (2000).
7. K. Bauer, D. Garbe, H. Surburg, Common Fragrance and Flavour Materials, New York, 1990.
8. Wilson R. Kirk Other's Encyclopedia of Chemical Technology vol. 4 (1991), John Wiley & Sons, New York p. 116
9. House H.O. Modern Synthetic Reactions (1972), W.A. Benjamin, Menlo Park
10. Carey F.A., and Sundberg R.J. Advanced Organic Chemistry (1977), Plenum Press, New York
11. Bartok M., and Lang K.L. In: Weissberger A., and Taylor E.C. (Eds). Chemistry of Heterocyclic Compounds (1985), Wiley, New York
12. Sreekumar R., Padmakurmar R., and Rugmini P. Tetrahedron Lett. 39 (1998) 5515
13. Smith G. Synthesis 8 (1984) 629
14. Bonini C. Tetrahedron 45 (1989) 2895-2904
15. Hudlicky M. Reductions in Organic Chemistry (1974), Ellis Horwood, Chichester
16. Eliel E.L., and Delmonte D.W. J. Am. Chem. Soc. 78 (1956) 3226
17. Mihaolovic M.L., Andrejevic V., and Milovanoic J. Helv. Chim. Acta 69 (1976) 2305
18. Ookawa A., and Soai H.D. Bull. Chem. Soc. Jpn. 60 (1987) 1813
19. Krishnamurthy S., Shubert R.M., and Brown H.C. J. Am. Chem. Soc. 95 (1973) 8486
20. Hutchings R.O., Taffer I.M., and Burgoyne W. J. Org. Chem. 46 (1981) 5214
21. Smith W.B. J. Org. Chem. 49 (1984) 3219
22. Fort Y., Vanderesse R., and Caubere P. Tetrahedrom Lett. 26 (1985) 3111
23. Ranu B.C., and Das A.R. J. Chem. Soc. Chem. Commun. (1990) 1334
24. Campelo J.M., Chakraborty R., and Marinas J.M. Synth. Commun. 26 3 (1996) 415-421
25. Dimitrova R., Minkov V., and Micheva N. Appl. Catal. 145 (1996) 49-55
26. Steilemann M., Armor J.N., and Hölderich W.F. Chem. Commun. (1999) 696-698
27. Weissermel K., and Arpe H.J. Química Orgánica Industrial (1981), S.A. Reverté
28. M.P. De Frutos, J.A. Delgado, I. Vic, EP 0943611 (1999).
29. Yamaguchi K., Ebitani K., and Kaneda K. J. Org. Chem. 64 (1999) 2966
30. Hölderich W.F., Hesse M., and Näuman F. Angew. Chem. Int. Ed. 27 (1988) 266
31. Mitsui S., Imaizumi S., Hisashige M., and Sugi Y. Tetrahedron 29 (1973) 4093
32. W.F. Hölderich, M. Goetz, L. Hupfer, German Patent 3,801,106 (1989).
33. W.F. Hölderich, M. Goetz, L. Hupfer, Chemical Abstract, 1990, 112,55217n.
34. W. Buechele, et al., German Patent DE19936208 (2001).
35. Bergadà O., Salagre P., Cesteros Y., Medina F., and Sueiras J.E. Appl. Catal. A 272 (2004) 125-132
36. Kirm I., Medina F., Rodríguez X., Cesteros Y., Salagre P., and Sueiras J.E. J. Mol. Catal. A: Chem. 239 (2005) 215-221
37. Benson J.E., Hwang H.S., and Boudart M. J. Catal. 30 (1973) 146
38. Linz A., Larsson P.-O., Skarman B., and Andersson A. Appl. Catal. B 34 (2001) 161-178
39. Aramendia M.A., Benítez J.A., Borau V., Jiménez C., Marinas J.M., Porras J.M., Ruiz J.R., and Urbano F.J. Langmuir 15 (1999) 1192-1197
40. Aramendia M.A., Benítez J.A., Borau V., Jiménez C., Marinas J.M., Porras J.M., Ruiz J.R., and Urbano F.J. Colloid Surf. A: Physicochem. Eng. Aspects 225 (2003) 137-147
41. McCabe R.W., Wong C., and Woo H.S. J. Catal. 114 (1988) 354
42. Choren E., Homez I., Zárraga J., and Buriel M. Rev. Téc. Ing. Univ. Zulia 22 (1999) 18
43. Finol D., Choren E., Arteaga A., Sánchez J., and Arteaga G. Rev. Téc. Ing. Univ. Zulia 15 (1992) 101
44. Marceau E., Che M., Sanit-Just J., and Tatibouët J.M. Catal. Today 29 (1996) 29
45. Hwang C.-P., and Yeh C.-T. J. Mol. Catal. A: Chem. 112 (1996) 295
46. Levy P., and Primet M. Appl. Catal. 70 (1991) 263
47. Miller J.T., Meyers B.L., Barr M.K., Modica F.S., and Koningsberger D.C. J. Catal. 159 (1996) 41-49
48. J.M. Waston, US Patent 3,927,110, (1975), to Cosden Oil & Chemical Company.
49. Surya Praskash G.K., Mathew T., Krishnaraj S., Marinez E.R., and Olah G.A. Appl. Catal. A 181 (1999) 283-288
50. W.F. Hölderich, et al., US Patent 5,225,602, BASF, 1993.
51. Kochkar H., Clacens J.M., and Figueras F. Catal. Lett. 78 1-4 (2002) 91-94
52. Imanaka T., Okamoto Y., and Teranishi S. Bull. Chem. Soc. Jpn. 45 (1972) 325
53. Okamoto Y., Imanaka T., and Teranishi S. Bull. Chem. Soc. Jpn. 47 (1973) 464
54. Fujitsu H., Shirahama S., Matsumura E., Takeshita K., and Mochida I. J. Org. Chem. 46 (1981) 2287-2290
55. Yadav V.G., and Chandalia S.B. Org. Proc. Res. Dev. 2 (1998) 294
56. Prinetto F., Manzoli M., Ghiotti G., Martínez Ortiz M.J., Tichit D., and Coq B. J. Catal. 222 (2004) 238-249