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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466784Generated: October 30, 2026

Epichlorohydrin → Diglycidyl ether

https://huagongshe.com/reaction/466784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
ProductDiglycidyl etherHCID 1670491.5%

Reaction Steps

To a mixture of 382 g (4.13 moles) of epichlorohydrin and 86 g (0.21 mole) of bis(1,1,1,3,3,3-hexafluoro-2-hydroxyisopropyl)cyclohexane (Compound A) obtained in Reference Example 2 were added 16.8 g (0.42 mole) of sodium hydroxide and 2 ml of water. The mixture was heated with stirring and reacted with reflux for 10 hours. The resulting sodium chloride was removed by filtration with use of a glass filter and the excess of epichlorohydrin was distilled off at a reduced pressure. The residue was checked by gel permeation chromatography (GPC) to find that the compounds of the formula (1) in which n was 0, 1 and 2 were contained in 93:6:1 (ratio of area on chromatogram). Conditions for GPC: column, Shodex, KF-801, KF-802, each 30 cm, solvent, chloroform. The reside was distilled to obtain 50 g of diglycidyl ether of the compound of the formula (1) wherein n was zero, namely Compound A. The ether had a boiling point of 138° to 150° C./1 mmHg. ##STR15##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157148
Source datasetuspto-grants-1992_10
ORD IDord-b6bba8379f9a47f8a20bf074e6b0a39c
Source noteuspto-grants-1992_10