Reacción #1063727

Ecuación de reacción

2-(benzo[b]thiophen-5-yl)oxirane

potassium tert-butoxide

ethylene glycol

ethyl acetate

→

1-(benzo[b]thiophen-5-yl)-2-(2-hydroxyethoxy)ethanol

Disolventes

dimethyl sulfoxide

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONthereto was added, in 1.5 hours
2. 2
   OtroThe organic layer was separated
3. 3
   ExtracciónThe aqueous layer was extracted twice each with 30 ml of ethyl acetate
4. 4
   LavadoThe combined organic layer was washed with water
5. 5
   Secadoa staturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate
6. 6
   OtroThe solvent was removed by distillation under reduced pressure
7. 7
   OtroThe residue was purified by column chromatography (eluant: chloroform/ethanol=20/1)

Procedimiento

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.

Fuente