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Updated: Jul 12, 2025

Protocol for the Synthesis of Ortho-trifluoromethoxylated Aniline Derivatives
Published on: January 19, 2016
AITF (4-acetamidophenyl triflimide) mediated synthesis of amides, peptides and esters
Eti Chetankumar1, Swetha Bharamawadeyar1, Chinthaginjala Srinivasulu1
1Peptide Research Laboratory, Department of Studies in Chemistry, Sneha Bhavan, Bangalore University, Jnana Bharathi, Bengaluru 560 056, India. hariccb@gmail.com.
Abstract:
A simple, broadly applicable protocol for amidation and esterification reactions is described. Thereby, 4-acetamidophenyl triflimide (AITF), a crystalline stable reagent, is employed for the activation of carboxylic acids. The use of AITF as a coupling agent is demonstrated in the synthesis of peptides, amides and esters under mild conditions in good to excellent yields. Notably, peptide segment condensations were also accomplished. A diverse array of synthetic protocols showcasing a broad substrate scope and good functional group compatibility were accomplished. Herein, we systematically summarized the use of AITF in peptide synthesis strategies.
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