Reacción #60424

Ecuación de reacción

1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

butyraldehyde

sodium triacetoxyborohydride

acetic acid

sodium hydrogencarbonate

→

1-butyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine

Rendimiento 75.7%

Disolventes

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   Extracciónthe mixture was extracted with ethyl acetate
2. 2
   SecadoThe organic layer was dried over anhydrous magnesium sulfate
3. 3
   Filtraciónthe desiccant was filtered
4. 4
   Concentraciónthe filtrate was concentrated under reduced pressure
5. 5
   OtroThe resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane)

Procedimiento

To a solution of 1-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine (300 mg, 1.00 mmol) prepared in Example (8b) in tetrahydrofuran (20 mL) were added butyraldehyde (107 mg, 1.49 mmol), sodium triacetoxyborohydride (420 mg, 1.99 mmol) and acetic acid (60 mg, 0.99 mmol) in that order, the mixture was stirred at room temperature for 13 hours and 30 minutes. After the reaction completed, saturated aqueous sodium hydrogencarbonate was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and then the desiccant was filtered and the filtrate was concentrated under reduced pressure. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 270 mg of 1-butyl-4-[2-(3,3,5,5-tetramethylcyclohexyl)phenyl]piperazine as a light yellow oil.

Fuente