Analysis of the positions of substitution of acetate and propionate groups in cellulose acetate–propionate by the reductive-cleavage method

Abstract

The degree of substitution (ds) and the distribution pattern of the two ester substituents in commercial samples of cellulose acetate–propionate (CAP) were determined by sequential neutral methylation, direct reductive cleavage, and in situ acetylation. When the reductive-cleavage reaction was conducted with 35 equiv (per anhydroglucose unit) of Et 3SiH, 70 equiv of MeSO 3SiMe 3, and 14 equiv of BF 3·OEt 2 at room temperature for seven days, the O-acetyl groups were converted to O-ethyl groups, and the O-propionyl groups were converted to O-propyl groups concurrent with reductive cleavage of the glycosidic linkages. Acetylation of the products gave 27 partially methylated, ethylated, and propylated 4- O-acetyl-1,5-anhydro- d-glucitol derivatives that were identified by GLC–CIMS (NH 3) and GLC–EIMS. Integration of the GLC profile and correction for molar response gave the mole percent of each product. From these data, the fractional degree of substitution for each ester at each position of the anhydroglucose unit was determined. The combined fractional degree of substitution of both esters at each position and the overall ds were also determined by sequential neutral methylation, acyl–ethyl exchange, and reductive cleavage, and the values so obtained were in good agreement with those derived by sequential neutral methylation and direct reductive cleavage.