Reacción #2985
ord-23a827758ec74998ac781f9b6412b1c4
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe amine precipitates
- 2workup.ADDITIONThereafter, 50 cm3 of chloroform are added
- 3workup.WAITThe medium is left
- 4workup.STIRRINGstirred for 15 minutes
- 5ExtracciónThe aqueous phase is extracted with 3 times 50 cm3 of chloroform
- 6LavadoThe organic phases are washed with water
- 7Secadodried over calcium chloride
- 8Otroevaporated
- 9OtroPurification of the products
- 10Otrois performed either by recrystallization or by column chromatography
Procedimiento
After 0.005 mol (equivalent to 1.26 g) of 3-(7-methoxy-1-naphthyl)propylamine hydrochloride has been dissolved in 20 cm3 of water, 0.015 mol of potassium carbonate is added. The amine precipitates. Thereafter, 50 cm3 of chloroform are added and 0.010 mol of acetyl chloride is added dropwise. The medium is left stirring for 2 hours. It is acidified with 2N of hydrochloric acid and then stirred for 15 minutes. The aqueous phase is extracted with 3 times 50 cm3 of chloroform. The organic phases are washed with water, dried over calcium chloride and evaporated. Purification of the products is performed either by recrystallization or by column chromatography.