Add time:07/15/2019         Source:sciencedirect.com

A method is described for the synthesis, purification and radiolabelling of 2-{6-(4-bromophenoxy)hexyl}oxirane-2-carboxylic acid. For the synthesis of this new agent, 6-(4-bromophenoxy)hexylbromide (1), synthesized by the treatment of 4-bromophenol with 1,6-dibromohexane under basic conditions, was converted to diethyl 6-(4-bromophenoxy)hexylmalonate (2), which, on alkaline hydrolysis, yielded ethyl 6-(4-bromophenoxy)hexylmalonate (3). Ethyl 8-(4-bromophenoxy)-2-methyleneoctanoate (4), prepared from the monoester (3), was oxidized with m-chloroperbenzoic acid to yield ethyl 2-{6-(4-bromophenoxy)hexyl}oxirane-2-carboxylate (5). The method of radiolabelling, based on the Cu(I)Cl-assisted nucleophilic exchange reaction, resulted in regioselective radiobromination with a 45% radiochemical yield.

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