Abstract
The epoxidation reaction of an α,β-unsaturated ketone (2-cyclohexen-1-one), that is, an electron deficient C=C bond was performed over as-prepared and calcined layered double hydroxides (LDHs) of both the hydrotalcite- and the hydrocalumite type. It was found that the as-prepared LDHs always performed better than the calcined derivatives. Among them, the CaFe-LDH was the most active. The optimum reaction temperature and the most suitable solvent were also found after performing several set of reactions.
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