The paper describes a new synthesis of cationic derivatives of polysac
charides. Epichlorohydrin is reacted with any tertiary amine in the pr
esence of the carbohydrate substrate in heterogeneous phase. The react
ion is catalysed by 1-methylimidazole or by 1,4-diazabicyclo[2.2.2]oct
ane, the latter being more effective. Concerning its efficacy this met
hod is comparable with the classical route, using glycidyltrimethylamm
oniumchloride. As in the case of most heterogeneous reactions, the acc
essibility of the substrate plays an important role, thus the reactivi
ty is increasing in the order cotton linters < sulphite pulp < potato
starch. In the course oi the reaction the yield approaches an equilibr
ium value, which is determined by the accessibility of the substrate.
It was also checked, whether carboxylic groups, which may be present i
n the carbohydrate, may react under the conditions applied, leading to
ester linkages of the ammonium functions. This possibility was falsif
ied by model investigations.