Reacción #1178396
ord-3172d48492684866a26c03fcf649f011
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added
- 2ExtracciónThe mixture was extracted with 100 ml diethyl ether for three times
- 3SecadoThe diethyl ether solution was dried with anhydrous magnesium sulfate over night
- 4Otrothe magnesium sulfate was removed by filtration
- 5OtroDiethyl ether was evaporated
- 6Otrothe raw product was purified by a silica gel column
Procedimiento
Into a 500 ml round-bottomed flask were added 150 ml THF, 5 ml water, 2.2 g potassium carbonate, 6 ml diethyl amine, and 5 g p-bromobenzyl bromide. The resultant mixture was refluxed for 12 h. The mixture was then cooled to room temperature, into which 6 ml concentrated HCl was added, followed by the addition of 150 ml water. The mixture was extracted with 100 ml diethyl ether for three times. The diethyl ether solution was dried with anhydrous magnesium sulfate over night and then the magnesium sulfate was removed by filtration. Diethyl ether was evaporated and the raw product was purified by a silica gel column using hexane/chloroform mixture (1:1 by volume) as the eluent. (p-bromobenzyl)diethyl amine (BBDA) was obtained in 74% yield (3.6 g).