Reacción #710488
ord-9b6368c4f43e4419ae61e9ff6c473a4f
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added
- 2OtroAfter separation
- 3Extracciónthe aqueous phase was extracted twice with dichloromethane
- 4LavadoThe combined organic phases were washed with 5 mL of water
- 5Secadodried over magnesium sulfate
- 6Filtraciónfiltered
- 7Concentraciónconcentrated
- 8Otroto yield to 0.150 g of crude material, which
- 9Otrowas purified by chromatography on silica gel
Procedimiento
0.16 g of N-{2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]ethylidene}-2-(trifluoromethyl)benzamide (Int-6) were diluted in 2 mL of methanol. 50 μL of sulfuric acid 99% were added. The reaction mixture was stirred at room temperature for 48 hours. A mixture of dichloromethane (10 mL) and water (5 mL) was added. After separation, the aqueous phase was extracted twice with dichloromethane. The combined organic phases were washed with 5 mL of water, dried over magnesium sulfate, filtered, concentrated to yield to 0.150 g of crude material, which was purified by chromatography on silica gel to yield 0.107 g (63%) of desired product N-{2-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]-1-methoxyethyl}-2-(trifluoromethyl)benzamide (Ia-111), [M+1]=427.