The invention discloses a method for synthesizing
bisphenol A diglycidyl ethers through
halogen-free epoxidation, which is characterized by comprising the following steps of: adding
bisphenol A diallyl ethers, a
solvent I and a
phosphotungstic acid quaternary ammonium salt catalyst into a reactor, adding a
hydrogen peroxide solution into the reactor while stirring, raising the temperature of a reactant to 30-80 DEG C, and reacting the obtained object for 5-24 hours at a temperature of 30-80 DEG C so as to obtain a reacted material; cooling the reacted material to
room temperature, separating an organic phase, after the separated organic phase is subjected to
distillation recycling so as to obtain an
organic solvent, uniformly stirring and mixing the rest material and
ethyl acetate, carrying out filtering on the obtained product, and after filter liquor is subjected to
distillation recycling so as to obtain
ethyl acetate, obtaining a coarse product; and carrying out
column chromatography on the coarse product by using a
solvent III so as to obtain
bisphenol A diglycidyl ethers. After the method disclosed by the invention is adopted, no organic
chlorine ion contains in the process of synthesis, a synthesized target product not only has no organochlorine heterogeneous
client base, but also is low in product
viscosity, good in performance, simple in process, easy to operate, high in safety, low in
pollution and strong in practicability.