Réaction #68004
ord-4a786edb6cba4750b7f60d17b93ce9d9
Équation de réaction
Réactifs
Aucun
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe solvent was removed under reduced pressure
- 2Extractionextracted with ethyl acetate
- 3LavageThe organic layer was washed sequentially with water
- 4Séchagean aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate
- 5Autrethe solvent was removed under reduced pressure
Mode opératoire
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.