Reaction of linear acetals RCH(OR')(2) (R = H, CH3, C2H5; R' = CH3, C2H5, C
3H7) with ethylene glycol in a neutral medium at 25 degrees C was studied b
y C-13 NMR spectroscopy. The equilibrium compositions of the reaction mixtu
res and their dependence on the reactant molar ratio were determined. It is
shown that under the experimental conditions used dimethoxymethane fails t
o react with ethylene glycol, and the reactions of the other acetals yield
much cyclic acetals, 1,3-dioxolanes. The reaction of 2-methyl-1,3-dioxolane
with methanol gives the same products as the reaction of 1,1-dimethoxyetha
ne with ethylene glycol.