4.6 Article

Synthesis of No-Carrier-Added 4-[18F]Fluorophenol from 4-Benzyloxyphenyl-(2-thienyl)iodonium Bromide

Journal

MOLECULES
Volume 16, Issue 9, Pages 7621-7626

Publisher

MDPI
DOI: 10.3390/molecules16097621

Keywords

fluorine-18; 4-[F-18]fluorophenol; diaryl iodonium salts; radiosynthesis; positron emission tomography

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4-[F-18]Fluorophenol is a versatile synthon for the synthesis of more complex radiopharmaceuticals bearing a 4-[F-18]fluorophenoxy moiety. In order to prepare 4-[F-18]fluorophenol in no-carrier-added (n.c.a.) form only a nucleophilic labelling method starting from [F-18]fluoride is suitable. In this paper a new, two step radiosynthesis starting from 4-benzyloxyphenyl-(2-thienyl) iodonium bromide and [F-18]fluoride with subsequent deprotection is described, yielding n.c.a. [F-18]fluorophenol in 34 to 36% radiochemical yield.

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