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Preparation of 4-Azido-2,6-diflurophenol Acetate, a Click Reagent
Published: 23 October 2011 by MDPI in The 15th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis
Abstract: The title compound was prepared from 2,6-difluorophenol in four steps. Acetylation, followed by nitration, reduction to the amine and diazotization/azide formation proceeded in the expected fashion. A copper-catalyzed Huisgen cyclization between the compound and phenylacetylene was carried out as a model and the triazole isolated. The propargyl ester of naproxen was prepared (naproxen/propargyl alcohol/carbodiimide) and the subsequent click reaction carried out. It is expected that this strategy will afford access to materials with dual biological activity.
Keywords: 2,6-difluorophenol, click chemistry