Reacción #80272

ord-f7bdde7295d34614a571b2a077a7bc7d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas dropwise added
  2. 2
    workup.STIRRINGthe mixture was further stirred at room temperature for 4 hours
  3. 3
    ConcentraciónIt was then concentrated under reduced pressure
  4. 4
    Otroto remove acetone
  5. 5
    workup.ADDITIONa saturated sodium bicarbonate aqueous solution was added
  6. 6
    ExtracciónThe mixture was extracted with ethyl acetate
  7. 7
    Otrothe aqueous layer was precipitated with 10% hydrochloric acid
  8. 8
    FiltraciónThe precipitated crystals were collected by filtration
  9. 9
    Lavadowashed with water

Procedimiento

0.6 g of 5-(4,6-dimethoxypyrimidin-2-yl)oxy-4-formyl-3-methylbenzothiophene was dissolved in 80 ml of acetone. While stirring the solution at room temperature, 0.6 g of potassium permanganate dissolved in 10 ml of water was dropwise added thereto over a period of 15 minutes, and the mixture was further stirred at room temperature for 4 hours. It was then concentrated under reduced pressure to remove acetone, and then a saturated sodium bicarbonate aqueous solution was added thereto to make the mixture alkaline. The mixture was extracted with ethyl acetate, and then the aqueous layer was precipitated with 10% hydrochloric acid. The precipitated crystals were collected by filtration and washed with water to obtain 0.47 g (yield: 76%) of the desired compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05616537uspto-grants-1997_04