Reacción #317135
ord-d5d8a7a4ea0742dfb82600e83318eccd
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1TemperaturaThe mixture was heated
- 2Temperaturato reflux for 4 hours
- 3Extracciónextracted with ether
- 4ExtracciónThe product was extracted into saturated aqueous sodium bicarbonate
- 5ExtracciónThis aqueous extract
- 6Extracciónextracted with ether
- 7ExtracciónThe organic extract
- 8Secadowas dried over magnesium sulfate
- 9Filtraciónfiltered
- 10Otroevaporated
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)