Reacción #46768
ord-1b4ca2bb93d942fea56fb0af7f9c5bd2
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroA 100 mL round bottom flask equipped with a stir bar
- 2Lavadowashed with water (3×100 mL)
- 3SecadoOrganic layer was dried over anhydrous sodium sulfate
- 4Concentraciónconcentrated under reduced pressure
Procedimiento
A 100 mL round bottom flask equipped with a stir bar was charged with CH2Cl2 (30 mL), 2-bromo-phenethylamine (1.0 g, 5.00 mmol) and triethylamine (684 μl, 5.05 mmol). The reaction solution was treated with menthoyl chloride (1.02 g, 5.05 mmol) in one portion and stirred at ambient temperature for 30 minutes. The reaction was diluted with CH2Cl2 (50 mL) and washed with water (3×100 mL). Organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a thick oil (1.8 g). Product was used for next step without purification.