Abstract
Arylhydrazones of dehydroacetic acid (DHA) underwent Vilsmeier–Haack reaction to generate the corresponding 1-aryl-4-formyl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)pyrazoles (1) with the pyrone moiety of the DHA remaining intact. However, when the reaction was performed using 1 equiv. of the reagent, compounds of 1-aryl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)pyrazoles (2a–2f) were obtained, which underwent smooth conversion to 1-aryl-4-formyl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)pyrazoles (1) on further treatment with another equivalent of the Vilsmeier–Haack reagent. This unreported observation suggests the intermediacy of 1-aryl-3-(4-hydroxy-6-methyl-2-oxo-2H-pyran-3-yl)pyrazoles (2) in Vilsmeier–Haack reactions of hydrazones with a pyrone moiety. Several analogous compounds were also prepared using arylhydrazones of DHA.Key words: dehydroacetic acid, pyrazoles, Vilsmeier–Haack reaction, 3-acetyl-4-hydroxy-6-methyl-2H-pyran-2-one.
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