Reacción #2348130
ord-e413f568739645b2a2c5c47fc11a3307
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL)
- 2OtroThe organic layer was separated
- 3Lavadowashed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine
- 4Secadodried over MgSO4
- 5OtroSolvent was removed under reduced pressure
- 6Otrothe crude product was purified by column chromatography
Procedimiento
4-Hydroxybenzoic acid (1.01 g, 7.31 mmol) and 4-aminophenol (1.19 g, 10.9 mmol) were dissolved in 15 mL of dry DMF. To the above solution EDCI (1.40 g, 7.31 mmoL) was added in one portion and the resulting mixture was stirred at rt overnight under nitrogen. The reaction mixture was then partitioned between EtOAc (200 mL) and water (200 mL). The organic layer was separated, washed consecutively with 1 N HCl, water, saturated sodium bicarbonate solution, water, and brine, and dried over MgSO4. Solvent was removed under reduced pressure and the crude product was purified by column chromatography using EtOAc in hexane as an eluent (10% to 20%) to give 580 mg (34% yield) of 4-hydroxy-N-(4-hydroxyphenyl)-benzamide. MS (ES) m/z: 230.04 (M+1).