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Benzylation of Toluene over Iron Modified Mesoporous Ceria

Department of Applied Chemistry, Cochin University of Science and Technology, Cochin-682022, Kerala, India

Received: 30 Jun 2012; Revised: 7 Nov 2012; Accepted: 10 Nov 2012; Published: 30 Dec 2012.
Editor(s): Istadi Istadi
Open Access Copyright (c) 2012 by Authors, Published by BCREC Group
Creative Commons License This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
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Abstract
Green chemistry has been looked upon as a sustainable science which accomplishes both economical and environmental goals, simultaneously.With this objective, we developed an alternative process to obtain the industrially important benzyl aromatics by benzylation of aromatics using benzyl chloride, catalysed by mesoporous solid acid catalysts. In this work mesoporous ceria is prepared using neutral surfactant which helped the calcination possible at a lower temperature enabling a higher surface area. Mesoporous ceria modified with Fe can be successfully utilized for the selective benzylation of toluene to more desirable product methyl diphenyl methane with 100% conversion and selectivity in 2 hours using only 50mg of the catalyst under milder condition. The reusability, regenerability, high selectivity, 100% conversion, moderate reaction temperature and absence of solvent, etc. make these catalysts to be used in a truly heterogeneous manner and make the benzylation reaction an environment friendly one. © 2012 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0)
Keywords: Benzylation of aromatics, Green chemistry, Lewis acidity, Solid mesoporous acids
Funding: University Grants Commission (India)

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  1. Friedel, C., and Crafts, J.M., (1877). Compt. Rend. Acad. Sci, Paris 84: 1292
  2. Rupa, V., Palanichami, A. (2008). Phenol Hydroxylation Using Fe/Al-MCM-41 Catalysts. Catal. Lett.120: 56-64. doi: 10.1007/s10562-007-9249-8
  3. Tanev, P. T., Pinnavaia, T. J., (1995), A Neutral Templating Route to Mesoporous Molecular Sieves. Science (New York, NY) 267 (5199 ): 865- 867. doi: 10.1126/science.267.5199.865
  4. Tanabe, K., Misono, M., Ono, Y., (1989), Solid Acids and Bases. Elsevier Science Publishers, Tokyo-Amsterdam, p.252
  5. Bradley, S.M., and Kydd, R.A., (1993), Chromium pillared montmorillonites: acidity and reactivity for cumene conversion. J Catal. 141: 239-249. doi: 10.1006/jcat.1993.1132
  6. Brauner, S., Emmette, P.H., Teller, E., (1938) Adsorption of Gases in Multimolecular Layers. J. Am. Chem. Soc., 60 (2): 309–319. doi: 10.1021/ja01269a023
  7. Tillirou, A.A., and Theocharis, C.R., (2008). Synthesis and Characterization of Mesoporous Cerium Oxide Prepared Using an Organic Base and a Templating Agent. Adsorption Science & Technology 26: 687-692. doi: 10.1260/026361708788251385
  8. Despande, A. B., Bajpai, A. R., Samant, S.D., (2001). The enhanced activity of Sb after supporting on K10 in the benzylation of benzene using benzyl chloride and benzyl alcohol. Appl. Catal. A: Gen., 209: 229-236. doi: 10.1016/S0926-860X(00)00777-8
  9. He, N., Bao, S., Xu, Q., (1998). Fe-containing mesoporous molecular sieves materials: very active Friedel-Crafts alkylation catalysts. Appl. Catal. A: Gen., 169: 29–36. doi: 10.1016/S0926-860X(97)00347-5

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