REACTION OF DICHLOROALLOSE UNITS IN A CHLORODEOXYCELLULOSE WITH LITHIUM-CHLORIDE UNDER HOMOGENEOUS CONDITIONS IN N,N-DIMETHYLACETAMIDE

The reaction of methyl 3,6-dichloro-3,6-dideoxy-beta-D-allopyranoside with lithium chloride in N,N-dimethylacetamide (DMA) was studied in re lation to the possible conversion of 3,6-dichloro-3,6-dideoxy-D-allose units in a chlorodeoxycellulose during synthesis in a LiCl-DMA solven t system. Methyl 3,6-dichloro-3,6-dideoxy-beta-D-glucoside was formed; the reaction was reversible and the equilibrium was on the glucoside side. GLC analysis of the hydrolyzates of chlorodeoxycellulose samples after treatment with LiCl showed that the dichloroallose units were p artly converted into 3,6-dichloro-3,6-dideoxy-D-glucose units. A kinet ic study showed that the rate of conversion of the dichloroallose unit into the dichloroglucose unit was lower than that of the dichloroallo side into the dichloroglucoside, and the amounts of the two units at e quilibrium were calculated to be close to each other. Based on the val ues of the kinetic parameters obtained, the conversion of the dichloro allose units into the dichloroglucose units during the chlorination of cellulose in LiCl-DMA was estimated to be negligibly small under typi cal reaction conditions.