The network formation process of the triethylamine-initiated reaction of 1,4-butanediol diglycidyl ether with cis-1,2-cyclohexanedicarboxylic anhydride has been investigated by conventional differential scanning calorimetry and temperature scanning Brillouin light scattering as a new experimental method far the estimation of the reaction’s conversion factor. The time-temperature evolution of the observed quantities (reaction enthalpy in the calorimetric measurements and hypersound velocity in the light scattering) reflects in both sets of experimental data, but results in different kinetic parameters obtained by the assumption of an Arrhenius behavior. These differences are ascribed to the relation of the observed properties with respect to the evolution of the reaction. The enthalpy production of the system observed in the calorimetric experiment is shown to be connected directly to the chemical reaction, whereas the change in the hypersound velocity measured by the light scattering method is sensitive to the solidification of the system.