تفاعل #834982

ord-7c25f9a433a94596837ca08a72d607fe

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىat 0-5° C
  2. 2
    أخرىto come to room temperature
  3. 3
    workup.STIRRINGstirred for 20 h
  4. 4
    استخلاصthe aqueous solution thoroughly extracted with dichloromethane (5×100 mL)
  5. 5
    غسيلThe combined organic layers were washed with water (2×200 mL), saturated sodium carbonate (2×200 mL)
  6. 6
    تجفيفdried (anhydrous sodium sulfate)
  7. 7
    أخرىAfter removal of the solvent
  8. 8
    أخرىthe residue was chromatographed over silica gel
  9. 9
    غسيلElution with 30% ethyl acetate in hexanes

الإجراء التجريبي

To an ice-cold mixture of methyl 3-amino-2-hydroxypropionate hydrochloride (19) (27.1 g, 0.17 mol) in water (100 mL) and dichloromethane (100 mL) was added sodium carbonate (19.82 g, 0.187 mol) and CuSO4. 5H2O (0.3 g, 1.2 mmol) with stirring. Triflylazide from experiment 10(B)(i) (crude, 44.6 g, 0.25 mol) was added dropwise keeping the reaction temperature at 0-5° C. Methanol (about 100 mL) was added until the reaction mixture became homogeneous. The reaction mixture was allowed to come to room temperature and then stirred for 20 h. Water (500 mL) was added and the aqueous solution thoroughly extracted with dichloromethane (5×100 mL). The combined organic layers were washed with water (2×200 mL), saturated sodium carbonate (2×200 mL), and then dried (anhydrous sodium sulfate). After removal of the solvent, the residue was chromatographed over silica gel. Elution with 30% ethyl acetate in hexanes furnished the product as a colorless oil (14.0 g; Yield: 57%) Rf 0.57 (30% ethyl acetate in hexanes).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07399460B2uspto-grants-2008_07