Reacción #2981
ord-930d75a478a44c1f993455a3cf0bd573
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
-10°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.WAITThe mixture is left
- 2workup.STIRRINGstirring for 30 minutes
- 3ExtracciónThe aqueous phase is extracted with 3 times 50 cm3 of dichloromethane
- 4Lavadothe organic phase is washed with 3 times 20 cm3 of 1N hydrochloric acid solution
- 5Secadowith water, dried over potassium carbonate
- 6Otroevaporated
- 7OtroThe oily residue is recrystallized
Procedimiento
In a 250-cm3 flask, 4 g of 2-(7-methoxy-1-naphthyl)ethanol are dissolved in 100 cm3 of dichloromethane, and 3.3 cm3 of triethylamine are added. The mixture is cooled in an ice bath at -10° C. and 2.75 g of mesyl chloride are then added dropwise and with stirring. The mixture is left stirring for 30 minutes. The aqueous phase is extracted with 3 times 50 cm3 of dichloromethane, and the organic phase is washed with 3 times 20 cm3 of 1N hydrochloric acid solution and then with water, dried over potassium carbonate and evaporated. The oily residue is recrystallized.