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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976545Generated: October 29, 2026

Ethylene Glycol → 1-(Benzo[b]thiophen-5-yl)-2-(2-hydroxyethoxy)ethanol

https://huagongshe.com/reaction/976545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantEthyl AcetateHCID 8857—
Reactant2-(Benzo[b]thiophen-5-yl)oxiraneHCID 15186629—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product1-(Benzo[b]thiophen-5-yl)-2-(2-hydroxyethoxy)ethanolHCID 53918729—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5.7 g of potassium tert-butoxide and 57 ml of ethylene glycol was heated to 80° C. thereto was added, in 1.5 hours, a solution of 18 g of 2-(benzo[b]thiophen-5-yl)oxirane dissolved in 30 ml of dimethyl sulfoxide. The resulting mixture was stirred at the same temperature for 30 minutes. The reaction mixture was added to a mixture of 120 ml of ice water and 80 ml of ethyl acetate. The organic layer was separated. The aqueous layer was extracted twice each with 30 ml of ethyl acetate. The extracts were combined with the previously separated organic layer. The combined organic layer was washed with water and a staturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluant: chloroform/ethanol=20/1) to obtain 9.1 g of 1-(benzo[b]thiophen-5-yl)-2-(2-hydroxyethoxy)ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612381
Source datasetuspto-grants-1997_03
ORD IDord-c92715acbdba4471878486ed7bb5f724
Source noteuspto-grants-1997_03