Reacción #949723

Ecuación de reacción

hydrochloric acid

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

hydrochloric acid

diethyl ether

p-toluenesulfonyl chloride

→

1-(benzo[b]thiophen-5-yl)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethanol

Rendimiento 51.9%

Disolventes

pyridine

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONTo the solution was added, at -25° C.
2. 2
   OtroThe organic layer was separated
3. 3
   ExtracciónThe aqueous layer was extracted with 30 ml of diethyl ether
4. 4
   LavadoThe combined organic layer was washed with water
5. 5
   Secadoa saturated 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: toluene/ethyl acetate=10/1)

Procedimiento

In 54 ml of pyridine was dissolved 9.0 g of 1-(benzo[b]thiophen-5-yl)-2-(2-hydroxyethoxy)ethanol. To the solution was added, at -25° C., 7.2 g of p-toluenesulfonyl chloride. The mixture was allowed to stand at 0°-5° C. for 24 hours and further at room temperature for 4 hours. The reaction mixture was added to a mixture of 103 ml of 6N hydrochloric acid, 50 ml of ice water and 100 ml of diethyl ether. The resulting mixture was adjusted to pH 2.0 with 6N hydrochloric acid. The organic layer was separated. The aqueous layer was extracted with 30 ml of diethyl ether. 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 was purified by column chromatography (eluant: toluene/ethyl acetate=10/1) to obtain 7.7 g of colorless oily 1-(benzo[b]thiophen-5-yl)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethanol.

Fuente