Reacción #5086
ord-15280f38c7e244d1bfa07303e59094ac
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónthe reaction mixture was extracted with 100 ml of ethyl acetate
- 2Lavadothe extract was washed 5 times with 100 ml of water
- 3Secadodried with anhydrous magnesium sulfate
- 4OtroThe solvent was removed by evaporation
- 5Otroto obtain the residue which
- 6Otrowas purified by means of a silica gel column chromatography (eluent: ethyl acetate: n-hexane=1:1)
Procedimiento
To a mixture of 1.50 g of 4-(3-chlorophenyl)-piperazine and 0.31 g of sodium hydride was added 2.4 ml of epichlorohydrin and the reaction mixture as stirred at room temperature for 30 minutes. After the reaction was completed, the reaction mixture was extracted with 100 ml of ethyl acetate, and the extract was washed 5 times with 100 ml of water, then dried with anhydrous magnesium sulfate. The solvent was removed by evaporation to obtain the residue which was purified by means of a silica gel column chromatography (eluent: ethyl acetate: n-hexane=1:1) to obtain 1.66 g of 4-(3-chlorophenyl)-1-(2,3-epoxypropyl)piperazine as in the form of an oily substance.