Reacción #632000
ord-641ed36f1ef745f48766df779a4afb37
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Otroat 45° C.
- 2OtroWhen the temperature of the mixture closed to 45° C.
- 3Otrowas then adjusted to 48° C
- 4workup.WAITAt 18 hours
- 5workup.WAITAt 24 hours the temperature was lowered to 35° C
- 6TemperaturaHeating
- 7workup.WAITwas stopped at 48 hours
- 8Temperaturathe reaction was slowly cooled down to room temperature (about 25° C.)
- 9workup.STIRRINGstirred overnight
- 10workup.WAITAt 66 hours
- 11ExtracciónThe mixture was extracted with MTBE (2×4 L)
- 12LavadoThe combined MTBE extracts were washed with 5% NaHCO3 (6×300 mL) and water (3×300 mL)
- 13Concentraciónconcentrated
Procedimiento
A solution of 5 L of 0.2M sodium borate buffer (pH 9) at 45° C. in a 20 L jacked reactor stirred at 400 rpm was treated with 3 L of DI water and 4 L of Savinase 16 L, type EX (Novozymes North America Inc.). When the temperature of the mixture closed to 45° C., the pH was adjusted to 8.5 with 10N NaOH. A solution of (1R,2S)/(1S,2R)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester (200 grams) in 2 L DMSO was added to the reactor over a period of 40 minutes via addition funnel. The reaction temperature was then adjusted to 48° C. After 2 hours, the pH was adjusted to pH 9.0 with 10N NaOH. At 18 hours, enantio-excess of the ester reached 72% and the pH was adjusted to 9.0 with 10N NaOH. At 24 hours the temperature was lowered to 35° C. At 42 hours the temperature was raised to 48° C. and the pH was adjusted to 9.0 with 10N NaOH. Heating was stopped at 48 hours and the reaction was slowly cooled down to room temperature (about 25° C.) and stirred overnight. At 66 hours, the pH of the reaction mixture was 8.6. The mixture was extracted with MTBE (2×4 L). The combined MTBE extracts were washed with 5% NaHCO3 (6×300 mL) and water (3×300 mL) and concentrated to give enantiomerically pure (1R,2S)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester as light yellow crystals (101A g; purity: 95.9% (210 nm, containing no acid; 98.6% ee).