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Iron(III) tosylate catalyzed acylation of alcohols, phenols, and aldehydes
Tetrahedron Letters (2012)
  • Ram S. Mohan, Illinois Wesleyan University
  • Neil J. Baldwin
  • Anna N. Nord
  • Brendan D. O’Donnell
Abstract
Iron(III) p-toluenesulfonate (tosylate) is an efficient catalyst for acetylation of alcohols, phenols, and aldehydes. The acetylation of 1° and 2° alcohols, diols, and phenols proceeded smoothly with 2.0 mol % of catalyst. However, the reaction worked well with only a few 3° alcohols. The methodology was also applicable to the synthesis of a few benzoate esters but required the use of 5.0 mol % catalyst. Aldehydes could also be converted into the corresponding 1,1-diesters (acylals) under the reaction conditions. Iron(III) tosylate is an inexpensive, and easy to handle, commercially available catalyst.
Keywords
  • Iron and its compounds,
  • Acylation,
  • Alcohols,
  • Diols,
  • Esters,
  • Green chemistry,
  • Phenols
Disciplines
Publication Date
Fall 2012
Publisher Statement
Tetrahedron Letters is published by Elsevier, see this link for more information.
Citation Information
Ram S. Mohan, Neil J. Baldwin, Anna N. Nord and Brendan D. O’Donnell. "Iron(III) tosylate catalyzed acylation of alcohols, phenols, and aldehydes" Tetrahedron Letters Vol. 53 Iss. 51 (2012) p. 6946 - 6949 ISSN: 0040-4039
Available at: http://works.bepress.com/ram_mohan/43/