تفاعل #631999

ord-08434296efb14e3e81912c021ab9d8d9

معادلة التفاعل

O=P([O-])([O-])[O-].[Na+].[Na+].[Na+]
sodium phosphate
[Na+].[OH-]
NaOH
[Na+].[OH-]
NaOH
[Na+].[OH-]
NaOH
C=C[C@H]1C[C@@]1(NC(=O)OC(C)(C)C)C(=O)OCC
(1S,2R)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester
C=C[C@@H]1C[C@]1(NC(=O)OC(C)(C)C)C(=O)OCC
(1R,2S)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester

المذيبات

ظروف التفاعل

درجة الحرارة
39°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added 511 grams of Alcalase 2.4 L (about 425 mL) (Novozymes North America Inc.)
  2. 2
    أخرىreached 39° C.
  3. 3
    درجة الحرارةThe reaction temperature was maintained at 40° C. for 24.5 hours during which time the pH of the mixture
  4. 4
    أخرىwas adjusted to 8.0 at the 1.5 hour and 19.5 hour time points
  5. 5
    درجة الحرارةthe reaction was cooled to room temperature (26° C.)
  6. 6
    استخلاصthe resulting mixture was extracted with MTBE (2×2 L)
  7. 7
    استخلاصThe combined MTBE extract
  8. 8
    غسيلwas washed with 5% NaHCO3 (3×100 mL), water (3×100 mL)
  9. 9
    تركيزconcentrated in vacuo

الإجراء التجريبي

To an aqueous solution of sodium phosphate buffer (0.1M, 4.25 L, pH 8) housed in a 12 Liter jacked reactor, maintained at 39° C., and stirred at 300 rpm, was added 511 grams of Alcalase 2.4 L (about 425 mL) (Novozymes North America Inc.). When the temperature of the mixture reached 39° C., the pH was adjusted to 8.0 by the addition of 50% NaOH in water. A solution of (1R,2S)/(1S,2R)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester (85 g) in 850 mL of DMSO was then added over a period of 40 minutes. The reaction temperature was maintained at 40° C. for 24.5 hours during which time the pH of the mixture was adjusted to 8.0 at the 1.5 hour and 19.5 hour time points using 50% NaOH in water. After 24.5 hours, the enantio-excess of the ester was determined to be 97.2%, and the reaction was cooled to room temperature (26° C.) and stirred overnight (16 hours) at which time the enantio-excess of the ester was determined to be 100%. The pH of the reaction mixture was then adjusted to 8.5 with 50% NaOH and the resulting mixture was extracted with MTBE (2×2 L). The combined MTBE extract was washed with 5% NaHCO3 (3×100 mL), water (3×100 mL), and then concentrated in vacuo to give the enantiomerically pure (1R,2S)N-Boc-1-amino-2-vinylcyclopropane carboxylic acid ethyl ester as light yellow solid (42.55 g; purity: 97% (210 nm, containing no acid; 100% enantiomeric excess (“ee”).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07935670B2uspto-grants-2011_05