Analysis of the positions of substitution of acetate and propionate groupsin cellulose acetate-propionate by the reductive-cleavage method

The degree of substitution (ds) and the distribution pattern of the two est er substituents in commercial samples of cellulose acetate-propionate (CAP) were determined by sequential neutral methylation, direct reductive cleava ge, and in situ acetylation. When the reductive-cleavage reaction was condu cted with 35 equiv (per anhydroglucose unit) of Et3SiH, 70 equiv of MeSO3Si Me3, and 14 equiv of BF3. OEt2 at room temperature for seven days, the O-ac etyl groups were converted to O-ethyl groups, and the O-propionyl groups we re converted to O-propyl groups concurrent with reductive cleavage of the g lycosidic linkages. Acetylation of the products gave 27 partially methylate d, ethylated, and propylated 4-O-acetyl-1,5-anhydro-D-glucitol derivatives that were identified by GLC-CIMS (NH3) and GLC-EIMS. Integration of the GLC profile and correction for molar response gave the mole percent of each pr oduct. From these data, the fractional degree of substitution for each este r at each position of the anhydroglucose unit was determined. The combined fractional degree of substitution of both esters at each position and the o verall ds were also determined by sequential neutral methylation, acyl-ethy l exchange, and reductive cleavage, and the values so obtained were in good agreement with those derived by sequential neutral methylation and direct reductive cleavage. (C) 1998 Elsevier Science Ltd. All rights reserved.