Issue 44, 2015

Expedient and efficient one pot synthesis of trifluoroethyl ethers from metal free 2,4,6-tris-(2,2,2-trifluoro-ethoxy)-[1,3,5] triazene

Abstract

An efficient synthesis of fluorinated alkyl and aryl ethers was achieved by the use of s-triazene derived fluorinated reagent 2,4,6-tris-(2,2,2-trifluoro-ethoxy)-[1,3,5] triazene (TriTFET). The procedure offers a very attractive alternative for the synthesis of fluorinated motifs that are found in various bioactive molecules. Moreover, TriTFET is a synthetic non-toxic, non-ozone depleting and stable reagent. All compounds were characterized by 1H, 13C and 19F NMR.

Graphical abstract: Expedient and efficient one pot synthesis of trifluoroethyl ethers from metal free 2,4,6-tris-(2,2,2-trifluoro-ethoxy)-[1,3,5] triazene

Supplementary files

Article information

Article type
Communication
Submitted
12 Jan 2015
Accepted
07 Apr 2015
First published
07 Apr 2015

RSC Adv., 2015,5, 35042-35045

Author version available

Expedient and efficient one pot synthesis of trifluoroethyl ethers from metal free 2,4,6-tris-(2,2,2-trifluoro-ethoxy)-[1,3,5] triazene

S. K. Mangawa, C. Sharma, A. kumar Singh and S. K. Awasthi, RSC Adv., 2015, 5, 35042 DOI: 10.1039/C5RA00618J

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