Reacción #949725

Ecuación de reacción

diethyl ether

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

methylamine

diethyl ether

hydrogen chloride ethanol

→

1-(benzo[b]thiophen-5-yl)-2-(N-methylaminoethoxy)ethanol hydrochloride

Disolventes

ethanol

acetone

Condiciones de reacción

Tratamiento posterior

1. 1
   TemperaturaThe resulting mixture was refluxed for 1 hour
2. 2
   OtroThe organic layer was separated
3. 3
   ExtracciónThe aqueous layer was extracted with 20 ml of diethyl ether
4. 4
   workup.ADDITIONTo the combined organic layer was added 20 ml of water
5. 5
   OtroThe aqueous layer was separated
6. 6
   ExtracciónThe organic layer was extracted with 10 ml of water
7. 7
   workup.ADDITIONTo the combined aqueous layer was added 30 ml of methylene chloride
8. 8
   OtroThe organic layer was separated
9. 9
   ExtracciónThe aqueous layer was extracted with 15 ml of methylene chloride
10. 10
    Secadothe combined organic layer was dried over anhydrous magnesium sulfate
11. 11
    OtroThe solvent was removed by distillation under reduced pressure
12. 12
    OtroThe residue thus obtained
13. 13
    workup.STIRRINGThe resulting mixture was stirred at room temperature for 1 hour
14. 14
    FiltraciónThe resulting crystals were collected by filtration

Procedimiento

In 15 ml of ethanol was dissolved 1.5 g of 1-(benzo[b]thiophen-5-yl)-1-(2-tetrahydropyranyloxy)-2-[2-(p-toluenesulfonyloxy)ethoxy]ethane- To the solution was added 4.9 ml of a 40% aqueous methylamine solution. The resulting mixture was refluxed for 1 hour. The reaction mixture was added to a mixture of 20 ml of ice water and 20 ml of diethyl ether. The organic layer was separated. The aqueous layer was extracted with 20 ml of diethyl ether. The extract was combined with the previously separated organic layer. To the combined organic layer was added 20 ml of water. The resulting mixture was adjusted to pH 1.5 with 6N hydrochloric acid and stirred at room temperature for 20 minutes. The aqueous layer was separated. The organic layer was extracted with 10 ml of water. The extract was combined with the previously separated aqueous layer. To the combined aqueous layer was added 30 ml of methylene chloride. The resulting mixture was adjusted to pH 11 with a 10% aqueous sodium hydroxide solution. The organic layer was separated. The aqueous layer was extracted with 15 ml of methylene chloride. The extract was combined with the previously separated organic layer and the combined organic layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was dissolved in 7 ml of acetone. To the solution was added 0.5 ml of a 5N dry hydrogen chloride-ethanol solution. The resulting mixture was stirred at room temperature for 1 hour. To the reaction mixture was added 7 ml of diethyl ether. The resulting crystals were collected by filtration to obtain 0.5 g of 1-(benzo[b]thiophen-5-yl)-2-(N-methylaminoethoxy)ethanol hydrochloride (compound No. 347).

Fuente