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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506491Generated: October 25, 2026

2-Ethylhexanol → 2-Ethylhexyl glycidyl ether

https://huagongshe.com/reaction/506491

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-EthylhexanolHCID 7720—
ReactantEpichlorohydrinHCID 7835—
Reactant1-Chloro-3-(2-ethyl-hexyloxy)-propan-2-olHCID 11816924—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product2-Ethylhexyl glycidyl etherHCID 17162—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a flame dried, 500 mL round bottomed flask equipped with an addition funnel charged with epichlorohydrin (15.62 g, 0.17 moles), is added 2-ethylhexanol (16.5 g, 0.127 moles) and stannic chloride (0.20 g, 0.001 moles). The reaction is kept under an argon atmosphere and warmed to 90° C. using an oil bath. Epichlorohydrin is dripped into the stirring solution over 60 minutes followed by stirring at 90° C. for 18 hours. The reaction is fitted with a vacuum distillation head and 1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol is distilled under 0.2 mm Hg. The 1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol (4.46 g, 0.020 moles) is dissolved in tetrahydrofuran (50 mL) and stirred at room temperature under an argon atmosphere. To the stirring solution is added potassium tert-butoxide (2.52 g, 0.022 moles) and the suspension is stirred at room temperature for 18 hours. The reaction is then evaporated to dryness, residue dissolved in hexanes and washed with water (100 mL). The hexanes phase is separated, dried with Na2SO4, filtered and evaporated to dryness to yield the crude 2-ethylhexyl glycidyl ether, which can be further purified by vacuum distillation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786067B2
Source datasetuspto-grants-2010_08
ORD IDord-782eb294a1f7454a834215436bab02a2
Source noteuspto-grants-2010_08