Reacción #1951067
ord-0e3cd0923ddf44ee93452bf59e22c56d
Ecuación de reacción
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe resulting solution was degassed with nitrogen
- 2Temperaturato cool to ambient temperature
- 3LavadoThe solution was washed with saturated sodium bicarbonate (350 mL)
- 4workup.DISTILLATIONThe crude product was purified by vacuum distillation (ca. 98° C., 0.6 Torr)
Procedimiento
4-Bromo-fluorobenzene (10.95 g, 62.57 mmol) was added to diethyl phosphite (8.86 mL, 68.8 mmol) at ambient temperature, followed by the addition of triethylamine (9.6 mL, 68.8 mmol). The resulting solution was degassed with nitrogen followed by the addition of tetrakis(triphenylphosphine)-palladium (3.0 g, 2.6 mmol). The resulting mixture was heated at 90° C. overnight. The reaction mixture was allowed to cool to ambient temperature and then ethyl acetate (350 mL) was added. The solution was washed with saturated sodium bicarbonate (350 mL) and then with saturated brine (2×350 mL). The crude product was purified by vacuum distillation (ca. 98° C., 0.6 Torr) to yield 8.956 g of 4-fluorophenyl-phosphonic acid diethyl ester (38.6 mmol, 94% yield) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.88-7.80 (m, 2H); 7.20-7.14 (m 2H); 4.22-4.04 (m, 4H); 1.36-1.32 (t, 6H); ESMS (m/z): M+1)+ found, 233.