Reacción #68004
ord-4a786edb6cba4750b7f60d17b93ce9d9
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroThe solvent was removed under reduced pressure
- 2Extracciónextracted with ethyl acetate
- 3LavadoThe organic layer was washed sequentially with water
- 4Secadoan aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate
- 5Otrothe solvent was removed under reduced pressure
Procedimiento
Into 3 mL of a 90% aqueous trifluoroacetic acid solution, 156 mg of 1-(1,3-dioxolan-2-ylmethyl)-4-chloroquinolin-2(1H)-one was dissolved, and the mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, and the reaction mixture was alkalified with an aqueous saturated sodium hydrogen carbonate solution, and then extracted with ethyl acetate. The organic layer was washed sequentially with water and an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to obtain 192 mg of a pale yellow oily substance, (4-chloro-2-oxoquinolin-1(2H)-yl)acetaldehyde.