Exclusive and complete introduction of amino groups and their N-sulfo and N-carboxymethyl groups into the 6-position of cellulose without the use of protecting groups

Abstract A new regioselective synthesis of 6-amino-6-deoxycellulose with a DS 1.0 (degree of substitution) at C-6, and its 6- N -sulfonated and its 6- N -carboxymethylated derivatives, without using protecting groups is described in this paper. The reaction conditions were optimized for preparing cellulose tosylate with full tosylation at C-6 and partial tosylation at C-2 and C-3. The nucleophilic substitution (S N ) reaction of the tosyl group by NaN 3 at low temperature of 50 °C in Me 2 SO was achieved completely at C-6, whereas the tosyl groups at C-2 and C-3 were not displaced. In contrast to this, at 100 °C the tosyl groups at C-6, and also those at C-2 and C-3, were replaced by azido groups. This regioselective reaction that depends on temperature makes it possible to reach a selective and quantitative S N reaction at C-6 at low temperatures. In the subsequent reduction step with LiAlH 4 , the azido group at C-6 was reduced to the amino group, and the tosyl groups at C-2 and C-3 were simultaneously completely removed. Also reported is a temperature-dependent, regioselective and complete iodination by nucleophilic substitution of the tosyl group at C-6 at 60 °C. At higher temperatures from 75 to 130 °C, substitution is also observed to occur at C-2. The selective iodination at 60 °C was employed to confirm the complete tosylation at C-6 of cellulose. The reaction products were identified by four different independent quantitative methods, namely 13 C NMR, elemental analysis, ESCA, and fluorescence spectroscopy. 6- N -Sulfonated and 6- N -carboxymethylated cellulose derivatives were also synthesized. The new derivatives are potent candidates for structure–function studies, e.g., studies in relation to regioselectively 2- N -sulfonated and 2- N -carboxymethylated chitosan derivatives.