Issue 43, 2011

A simple, rapid procedure for nucleophilic radiosynthesis of aliphatic [18F]trifluoromethyl groups

Abstract

A procedure for the radiosynthesis of aliphatic [18F]trifluoromethyl groups by reacting 1,1-difluorovinyl precursors with [18F]fluoride ions, resulting in the equivalent of direct nucleophilic addition of H[18F]F, has been developed. A variety of 18F-labelled model compounds were then obtained and two potential [18F]radiotracers were synthesised by a two step process starting from 1,1-difluorovin-2-yl 4-toluenesulfonate. The method is widely applicable for the synthesis of novel radiotracers in high radiochemical yields and good specific activity.

Graphical abstract: A simple, rapid procedure for nucleophilic radiosynthesis of aliphatic [18F]trifluoromethyl groups

Supplementary files

Article information

Article type
Communication
Submitted
27 Aug 2011
Accepted
29 Sep 2011
First published
11 Oct 2011

Chem. Commun., 2011,47, 11873-11875

A simple, rapid procedure for nucleophilic radiosynthesis of aliphatic [18F]trifluoromethyl groups

P. J. Riss and F. I. Aigbirhio, Chem. Commun., 2011, 47, 11873 DOI: 10.1039/C1CC15342K

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