Preparation of completely C6-carboxylated curdlan by catalytic oxidation with 4-acetamido-TEMPO.

Abstract Pure (1→3)-β-polyglucuronic acid sodium salt was prepared from curdlan by oxidation with 4-acetamido-TEMPO/NaClO/NaClO 2 in water at pH 4.7 and 35 °C. The oxidation conditions, including the reaction time and amounts of reagents added, were optimized for the preparation of (1→3)-β-polyglucuronic acids with high molecular weights. The primary C6 hydroxyl groups of curdlan were completely oxidized to the corresponding C6-carboxylates using a one- or two-step reaction process by controlling the oxidation conditions, thus providing pure (1→3)-β-polyglucuronic acids consisting only of d -glucuronosyl units. Unfortunately, however, the increased amounts of reagents and long reaction time led to significant depolymerization of the curdlan during the oxidation process, and the resulting (1→3)-β-polyglucuronic acids had weight-average degrees of polymerization of 340–360. The 13 C and 1 H NMR chemical shifts of the products were successfully assigned using pure (1→3)-β-polyglucuronic acid.