Etracker Debug:
	et_pagename = "Recyclable Catalysis|recat|C|[EN]"
	
        
Jump to ContentJump to Main Navigation

Recyclable Catalysis

1 Issue per year


VERSITA Emerging Science

Open Access

Open Access

Amberlyst-15 catalyzed acetylation of phenols and alcohols under solvent free conditions

Manoj A. Pande1 / Shriniwas D. Samant1

1Department of Chemistry, Institute of Chemical Technology, N. M. Parikh Road, Matunga, Mumbai - 400019, India

©2012 Versita Sp. z o.o.. This content is open access.

Citation Information: Recyclable Catalysis. Volume 1, Pages 6–9, ISSN (Online) 2084-7629, DOI: 10.2478/recat-2012-0002, August 2012

Publication History

Published Online:
2012-08-23

Abstract

Amberlyst-15 has been found to be an efficient reusable heterogeneous catalyst for acetylation of phenols and alcohols under solvent free conditions.

Keywords: Acetylation; Phenols; Alcohols; Acetic anhydride; Solvent free; Amberlyst-15; Heterogeneous catalyst

  • A. K. Chakraborti, M. K. Nayak, L.. Sharma, J. Org. Chem. 67, 1776 (2002)

  • T. W. Greene, P. G. M. Greene and Wuts, Protective Groups in Organic Synthesis (3rd edn.), Wiley, New York, (1999)

  • M.A. Malden, Protective Groups in Organic Synthesis (1st edn.), Blackwell Science Inc. (1999)

  • A. K. Chakraborti, M. K. Nayak, L. Sharma, J. Org. Chem. 64, 8027 (1999).

  • T. Sano, K. Ohashi, T.Oriyama, Synthesis 7, 1141 (1999)

  • R. I. Zhdanov, S. M. Zhenodarova, Synthesis 4 , 222 (1977)

  • E. F. V. Scriven, Chem Soc Rev. 12, 129 (1983)

  • E. Vedejs, N. S. Bennett, L. M. Conn, S. T. Diver, M. Gingras, S. Lin, P. A. Oliver, M. J. Peterson, J. Org Chem., 58, 7286 (1993)

  • A. C. Cope, E. C. Herrich, Org. Synth Coll Vol. IV. John Wiley and Sons, Inc., New York. (1963)

  • S. Chandrasakhar, T. Ramachander, M.Takhi, Tetrahedron Lett., 39, 3263 (1998)

  • S. K. De, Tetrahedron Lett., 45, 2919 (2004)

  • M.H. Sarvari, H. Sharghi. Tetrahedron, 61, 10903 (2005)

  • K. Jeyakumar, D. K. Chand, J. Mol. Catal. A: Chem., 255, 275 (2006)

  • T–S. Jin, Y –R. Ma, Z –H. Zhang, T –S. Li, Synth. Commun., 28, 3173 (1998)

  • A.K. Chkraborti, R. Gulhane, Chem Commun., 15, 1896 (2003)

  • F. Shirini, M. A. Zolfigol, K. Mohammadi, Bull Korean Chem Soc., 25, 325 (2004)

  • R. Kumareswaran, K. Pachamuthu, Y. D. Vankar, Synlett., 11, 1652 (2000)

  • R. Ghosh, S. Maiti, A. Chakraborty, Tetrahedron Lett.,46, 147 (2005)

  • A.N. Parvulescu, B. C.Gagea, G. Poneelet, V. I. Parvulescu, Appl. Catal. A. : Gen. 301, 133 (2006)

  • B.C. Ranu, P. Dutta, A. Sarkar, J. Chem. Soc., Perkin Trans. 1. 14, 2223 (2000)

  • M.L. Kantam, Aziz P Khatiza, R. Likhar, Catal. Commun. 7, 484 (2006)

  • G.P. Romanelli, D. O. Bennardi, J. C. Autino, G. T. Baronetti and H. J. Thomas E-Journal of Chemistry 5, 641 (2008)

  • (a) M.A. Harmer, Industrial processes using solid acid catalysts, in Handbook of Green Chemistry and Technology; J. H. Clark, D. J. Macquarris, eds.; Blackwell Publishers London. (2002) (b) S. B. Patil, P. R. Singh, M. P. Surpur, S. D. Samant, Synth. Commun., 37, 1659 (2007) (c) M. P. Surpur, P. R. Singh, S.B. Patil, & S.D. Samant, Synth. Commun., 37, 1965 (2007) (d) M. A. Pande, S. D. Samant, Synth. Commun., 41, 754 (2011) (e) A. Chakrabarti, M. M. Sharma, React. Polym., 20, 1 (1993)

  • A. Shaabani, A. Rahmati, Z. Badri, Catal. Commun., 9, 13 (2008)

Comments (0)

Please log in or register to comment.