Reacción #640535
ord-fe9f513d4eda4487a469911dcbe3d1d3
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe solvents were removed under reduced pressure at 40° C.
- 2workup.DISSOLUTIONthe residue dissolved in ethyl acetate (approx. 1 L)
- 3LavadoThe solution was washed sequentially with 1M potassium hydrogen sulfate, saturated sodium bicarbonate
- 4SecadoAfter drying over anhydrous magnesium sulfate
- 5Filtraciónfiltering
- 6Otrothe solution was removed under reduced pressure
- 7workup.ADDITIONTo the resulting oil was added hexane (approx. 1 L)
- 8TemperaturaAfter cooling to room temperature
- 9Otrothe solids were collected
- 10Lavadowashed with 2 L of hexane
- 11OtroThe resulting solid was recrystallized from hot ethyl acetate and hexane
Procedimiento
To a solution of 75.0 g (0.226 mol) of N-benzyloxycarbonyl-L-phenylalanine chloromethyl ketone in a mixture of 807 mL of methanol and 807 mL of tetrahydrofuran at −2° C., was added 13.17 g (0.348 mol, 1.54 equiv.) of solid sodium borohydride over one hundred minutes. The solvents were removed under reduced pressure at 40° C. and the residue dissolved in ethyl acetate (approx. 1 L). The solution was washed sequentially with 1M potassium hydrogen sulfate, saturated sodium bicarbonate and then saturated sodium chloride solutions. After drying over anhydrous magnesium sulfate and filtering, the solution was removed under reduced pressure. To the resulting oil was added hexane (approx. 1 L) and the mixture warmed to 60° C. with swirling. After cooling to room temperature, the solids were collected and washed with 2 L of hexane. The resulting solid was recrystallized from hot ethyl acetate and hexane to afford 32.3 g (43% yield) of N-benzyloxycarbonyl-3(S)-amino-1-chloro-4-phenyl-2(S)-butanol, mp 150-151° C. and M+Li+=340.