摘要
Benzohydroxamic acid reacts with dimethyl acetylenedicarboxylate in the presence of 10 mol% NaOAc to gen- erate （E）-N-（1,4-dimethoxy-l,4-dioxobutan-2-ylidene）-l-phenylcarboxamide oxide in good-to-excellent yield in water at room temperature for 2 h, which supplies a simple, efficient and environmentally friendly method to syn- thesize a wide range of nitrones. The benefits of this strategy not only conform to the requirment of green chemisty, but also possess atom economy.
Benzohydroxamic acid reacts with dimethyl acetylenedicarboxylate in the presence of 10 mol% NaOAc to gen- erate （E）-N-（1,4-dimethoxy-l,4-dioxobutan-2-ylidene）-l-phenylcarboxamide oxide in good-to-excellent yield in water at room temperature for 2 h, which supplies a simple, efficient and environmentally friendly method to syn- thesize a wide range of nitrones. The benefits of this strategy not only conform to the requirment of green chemisty, but also possess atom economy.
