Reacción #46768

ord-1b4ca2bb93d942fea56fb0af7f9c5bd2

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroA 100 mL round bottom flask equipped with a stir bar
  2. 2
    Lavadowashed with water (3×100 mL)
  3. 3
    SecadoOrganic layer was dried over anhydrous sodium sulfate
  4. 4
    Concentraciónconcentrated 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07741355B2uspto-grants-2010_06