Article ID Journal Published Year Pages File Type
5274186 Tetrahedron Letters 2008 4 Pages PDF
Abstract

The hydroxylation of β-ketoesters was studied using simple iron catalysts and 30 wt % hydrogen peroxide as the terminal oxidant. The highest activity and yield were achieved in the presence of iron(III) chloride. Cyclic β-ketoesters could be smoothly hydroxylated in 75-90% yield. For linear β-ketoester and β-ketoamide, the chloro-substituted products were obtained.

Graphical abstractThe selective hydroxylation of β-ketoesters was realized using hydrogen peroxide as oxidant catalyzed by iron(III) chloride. 75-90% yield could be achieved for the hydroxylation of cyclic ketoesters.Download full-size image

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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