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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362965Generated: October 27, 2026

Ethylene Glycol → 2-(2-Hydroxyethoxy)-1-(1-naphthyl)ethanol

https://huagongshe.com/reaction/362965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactant2-(Naphthalen-1-yl)oxiraneHCID 6454366—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
Product2-(2-Hydroxyethoxy)-1-(1-naphthyl)ethanolHCID 53885279—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4.5 g of potassium tert-butoxide and 45 ml of ethylene glycol was heated to 80° C. Thereto was dropwise added 13.7 g of 2-(1-naphthyl)oxirane in 1 hour. The resulting mixture was stirred for 1 hour at the same temperature. The reaction mixture was cooled and added to a mixture of 50 ml of ethyl acetate and 50 ml of ice water. The organic layer was separated. The aqueous layer was extracted twice each with 20 ml of ethyl acetate. The extracts were 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: toluene/ethyl acetate=1/3) to obtain 8.3 g of 2-(2-hydroxyethoxy)-1-(1-naphthyl)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872117
Source datasetuspto-grants-1999_02
ORD IDord-34186a21514f40a1b5212375be594f47
Source noteuspto-grants-1999_02