Reacción #68005

ord-10318cf545b342af92eebf4bf6c259ea

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvent was removed under reduced pressure
  2. 2
    Extracciónextracted with ethyl acetate
  3. 3
    LavadoThe organic layer was washed sequentially with water
  4. 4
    Secadoan aqueous saturated sodium chloride solution and dried over anhydrous magnesium sulfate
  5. 5
    Otrothe solvent was removed under reduced pressure

Procedimiento

Into 3 mL of a 90% aqueous trifluoroacetic acid solution, 361 mg of 1-(1,3-dioxolan-2-ylmethyl)-3-methylquinolin-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 354 mg of a pale yellow oily substance, (3-methyl-2-oxoquinolin-1(2H)-yl)acetaldehyde.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524738B2uspto-grants-2013_09