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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255251Generated: October 30, 2026

Epichlorohydrin → Diglycidyl ether

https://huagongshe.com/reaction/2255251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventWaterHCID 962—
ProductDiglycidyl etherHCID 16704—

Reaction Conditions

Temperature52.5 °C

Reaction Steps

The reaction product of (a), 1 liter of epichlorohydrin and 20 gm of benzyltrimethylammonium chloride (BTMAC) dissolved in 12 ml of water are charged to a 2 liter 3-neck round bottom flask equipped with a mechanical stirrer, thermometer, thermoregulator, condenser, Dean-Stark Trap and dropping funnel. The mixture is then heated to about 50 to 55° C. at high vacuum of 70 torr with stirring resulting in a vigorous reflux of the epichlorohydrin. 109 gm of NaOH (50% solution) is slowly added to the mixture over a period of 2 hours. The water/epichlorohydrin mixture is removed by distillation as soon as the azeotrope is formed. Upon completion of the addition, the epichlorohydrin is returned to the reaction mixture and the reaction is allowed to continue for an additional 1.5 hours. The reaction mixture is then cooled to room temperature and washed with 300 ml of ice water and separated. The organic layer is then washed with another 300 ml of water and the pH adjusted to about 5-6 using 10% aqueous acetic acid. The organic layer is then washed a third time with 300 ml of water and separated. The epichlorohydrin is then removed by distillation at reduced pressure (from 70 to 2 torr). The final distillation condition about less than 5 torr/110° C. The distillation is continued until no volatile could be distilled to ensure the complete removal of the epichlorohydrin. The yield is 330 gm. The epoxy value is 0.306 eq/100 g and the viscosity is 1310 cps at 25° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05239093
Source datasetuspto-grants-1993_08
ORD IDord-10a583b4cd644ee390909cf057f2a293
Source noteuspto-grants-1993_08