Reacción #360626

ord-d1e19e911cc84bcdaa396a444ef8cb5d

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was heated
  2. 2
    Temperaturato reflux for 4 hours
  3. 3
    Extracciónextracted with ether
  4. 4
    ExtracciónThe product was extracted into saturated aqueous sodium bicarbonate
  5. 5
    ExtracciónThis aqueous extract
  6. 6
    Extracciónextracted with ether
  7. 7
    ExtracciónThe organic extract
  8. 8
    Secadowas dried over magnesium sulfate
  9. 9
    Filtraciónfiltered
  10. 10
    Otroevaporated

Procedimiento

To a stirred solution of 2-fluoro-4-hydroxybenzonitrile (20.00 g, 145.9 mmol) in 160 mL of water, was added 50% aqueous sodium hydroxide (40.00 g, 500.0 mmol). The mixture was heated to reflux for 4 hours, cooled to room temperature, poured into iced concentrated hydrochloric acid, and extracted with ether. The product was extracted into saturated aqueous sodium bicarbonate and the ether layer discarded. This aqueous extract was acidified with concentrated hydrochloric acid and extracted with ether. The organic extract was dried over magnesium sulfate, filtered, and evaporated to give a white solid (22.90 g) of 2-fluoro-4-hydroxybenzoic acid in 100% yield. 1H NMR (300 MHz, CD3COCD3) δ (ppm): 9.80 (b, 1H), 7.87 (t, 1H), 6.77 (dd, 1H), 6.66 (dd, 1H). 19F-NMR (300 MHz, CD3COCD3) δ (ppm): −108.13 (s, decoupled). 2-Fluoro-4-hydroxybenzonitrile: 1H-NMR (300 MHz, CD3COCD3) δ (ppm): 7.61 (t, 1H), 6.81 (m, 2H), 5.80 (b, 1H). 19F-NMR (300 MHz, CD3COCD3) δ (ppm): −108.82 (s, decoupled)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07456315B2uspto-grants-2008_11