Carboxymethyl cellulose (CMC) was treated in a dipolar-aprotic solvent
like N,N-dimethylacetamide, or dimethylsulfolxide (DMSO) with p-tolue
nesulfonic acid yielding a high reactive gel-suspension of the polymer
. This mixture allows a direct esterification of free hydroxyl groups
of CMC as exemplified by acylation with carbonic acid chlorides, or an
hydrides, and with isocyanates as well as by sulphation, phosphating a
nd silylation. The products characterized by elemental analysis and FT
IR spectroscopy possess a high degree of functionalization.