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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257542Generated: October 27, 2026

Ethylene Glycol → 1-(4-Benzyloxyphenyl)-2-(2-hydroxyethoxy)ethanol

https://huagongshe.com/reaction/2257542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantHydrochloric AcidHCID 313—
Reactant2-[4-(Benzyloxy)phenyl]oxiraneHCID 13248717—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product1-(4-Benzyloxyphenyl)-2-(2-hydroxyethoxy)ethanolHCID 53839145—

Reaction Conditions

Temperature80 °C

Reaction Steps

9.5 g of potassium tert-butoxide was added to 92 ml of ethylene glycol. The mixture was heated to 80° C. Thereto was dropwise added, in 3 hours, a solution of 34.7 g of 2-(4-benzyloxyphenyl)oxirane dissolved in 220 ml of dimethyl sulfoxide. The resulting mixture was stirred for 30 minutes at the same temperature. The reaction mixture was cooled and added to a mixture of 1 liter of ice water and 600 ml of ethyl acetate. The resulting mixture was adjusted to pH 7 with 6N hydrochloric acid. The organic layer was separated. The aqueous layer was extracted with 200 ml of ethyl acetate. The extract was combined with the previously separated organic layer. The combined organic layer was washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant:chloroform/ethanol=10/1) to obtain 25 g of 1-(4-benzyloxyphenyl)-2-(2-hydroxyethoxy)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658904
Source datasetuspto-grants-1997_08
ORD IDord-b5e87a886c304834b7085c5e4a074a02
Source noteuspto-grants-1997_08