Journal of the Chinese Chemical Society · 2009 · 20 citations · 35 references
Natural SciencesChemical EngineeringChemistryCatalysisOrganic ChemistryReaction EngineeringCarbonyl ChemistryCatalyst DesignCatalyst PreparationCatalyst SynthesisCatalytic MechanismsCatalytic Reaction EngineeringAmino Carbonyl ReactionCatalyst Development For SynthesisCatalyst MechanismsCatalyst OptimizationMild Reaction ConditionsRecycle StrategiesRoom-temperature SynthesisSelectivity
Abstract Sulfamic acid was used as a catalyst in the synthesis of β‐amino carbonyl compounds from amines, acetophenone and aldehyde. The reaction was carried out at room temperature. High selectivity, mild reaction temperature, cost‐effective catalyst, simple product separation and catalyst recycle were notable achievements in the reaction. Another feature was that the reaction could be performed on a relatively larger scale to the model reaction (50 times), which also gave good yields. In particular, the first preparation of β, β'‐diamino diketone derivatives via the direct coupling of amines, acetophenone and isophthalic aldehyde promoted by sulfamic acid has been developed.
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