Reacción #303677
ord-fe21fc11dc864a748873268ab9a1da4b
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1LavadoThe organic layer is washed with water (3×)
- 2SecadoThe combined organic extracts are dried (Na2SO4)
- 3Concentraciónconcentrated under reduced pressure
- 4OtroThe solids are triturated with ether
Procedimiento
4-Amino-3-chloro-5-nitro-2-phenylamino-benzoic acid methyl ester 5c (0.50 g, 1.55 mmol) is dissolved into 2:1 EtOH/MeOH (15.5 mL). Saturated aqueous NH4Cl (15 mL), Zn powder (1.02 g, 15.6 mmol), and THF (10 mL) are added. After stirring for 20 hours, the reaction mixture is diluted with CH2Cl2/THF and water. The organic layer is washed with water (3×). The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The solids are triturated with ether to give 0.32 g (70%) clean desired product.