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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097Generated: October 26, 2026

Epichlorohydrin → 10-(2-Ethylhexyloxy)decyl glycidyl ether

https://huagongshe.com/reaction/1097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant10-(2-Ethylhexyloxy)decanolHCID 19694647—
CatalystTetrabutylammonium BromideHCID 74236—
SolventHexaneHCID 8058—
Product10-(2-Ethylhexyloxy)decyl glycidyl etherHCID 1969463582.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A 200-ml flask equipped with a stirrer, reflux tube and dropping funnel was charged with 24.8 g (87 mmol) of 10-(2-ethylhexyloxy)decanol, 17.7 g (0.191 mol) of epichlorohydrin, 1.4 g (4.4 mmol) of tetrabutylammonium bromide and 25 ml of hexane. While stirring the mixture at 40° C., 29.2 g (0.35 mol) of a 48% aqueous solution of NaOH were added dropwise over 3 hours. After completion of the dropping, the stirring was continued further for 2 hours at 40° C. After the resultant reaction mixture was washed with water, and the solvent was distilled off under reduced pressure, the resultant residue was purified by column chromatography on silica gel, thereby obtaining 24.6 g (yield: 82.6%) of 10-(2-ethylhexyloxy)decyl glycidyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723497
Source datasetuspto-grants-1998_03
ORD IDord-aca60743900142f7968a0bb1a46a2668
Source noteuspto-grants-1998_03