Reacción #60453
ord-369d6936f64943aba1f9b932445c8d80
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1LavadoThe separated organic layer was washed with water and brine in that order
- 2Secadodried over anhydrous sodium sulfate
- 3FiltraciónThe desiccant was filtered off
- 4Concentraciónthe filtrate was concentrated under reduced pressure
- 5OtroThe residue was dried under reduced pressure
Procedimiento
A mixture of 4-[4-bromo-2-(4,4-dimethylcyclohexyl)phenyl]piperazine-1-carboxylic acid t-butyl ester (1.5 g, 3.32 mmol) produced in Example (3e), trifluoroacetic acid (3 mL, 38.7 mmol) and dichloromethane (6 mL) was stirred for 2 hours and 30 minutes at room temperature. Saturated aqueous solution of sodium carbonate was added to the reaction mixture and extraction was performed with ethyl acetate. The separated organic layer was washed with water and brine in that order and then dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The residue was dried under reduced pressure to give 1.21 g of a crude product of the title compound as a brown oil.