Reacción #1447100
ord-e21fe3cf2f8d43e1b161a10802d46379
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONcharged with a stir bar
- 2Otromaintains below 10° C
- 3workup.STIRRINGthe resulting mixture is stirred overnight at 100° C
- 4workup.STIRRINGthe mixture is stirred for another h at 100° C
- 5OtroThe methanol fraction is evaporated
- 6workup.ADDITIONwater (200 mL) is added to the residue
- 7Extracciónthe resulting mixture is extracted with ethyl acetate
- 8LavadoThe combined organic extracts are washed twice with water, twice with brine
- 9Secadodried (MgSO4)
- 10OtroThe solvent is evaporated
- 11Lavadothe residue is washed with methanol
- 12OtroThe insoluble residue is separated by filtration
- 13Otrodried
- 14Otroto give the white product
Procedimiento
KOtBu (11.8 g) is added to a flask charged with a stir bar and dry NMP (40 mL) and chilled to −10° C. under argon atmosphere. A solution of ethyl (4-ethyl-phenyl)-acetate (10.1 g) and 1-bromo-4-cyano-3,5-difluoro-benzene (11.5 g) in NMP (40 mL) is added at such a rate that the reaction temperature maintains below 10° C. After stirring for 1 hour at room temperature, methanol (50 mL) and 1 M aqueous sodium hydroxide solution (39 mL) are added and the resulting mixture is stirred overnight at 100° C. Then, 4 M aqueous hydrochloric acid (100 mL) is added and the mixture is stirred for another h at 100° C. The methanol fraction is evaporated, water (200 mL) is added to the residue and the resulting mixture is extracted with ethyl acetate. The combined organic extracts are washed twice with water, twice with brine and dried (MgSO4). The solvent is evaporated and the residue is washed with methanol. The insoluble residue is separated by filtration and dried to give the white product.