반응 #5083

ord-acac8f88fae84d0d92a648b8d5b90be2

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타followed by flash evaporation to dryness at room temperature
  2. 2
    기타The residue was partitioned between dichloromethane (3×300 ml) and saturated NaCl (aq, 300 ml)
  3. 3
    건조dried over anhydrous Na2SO4, flash
  4. 4
    기타evaporated to dryness (dry weight=8.1 g)
  5. 5
    기타purified over E

실험 절차

Acetic anhydride (45 ml) was added to a stirring solution of Virginiamycin M1 (6.5 g) in anhydrous pyridine (45 ml) at room temperature. After 30 minutes, ice-cold methanol (85 ml) was added in portions. Stirring was continued for 20 more minutes followed by flash evaporation to dryness at room temperature. The residue was partitioned between dichloromethane (3×300 ml) and saturated NaCl (aq, 300 ml). The organic layers were pooled, dried over anhydrous Na2SO4, flash evaporated to dryness (dry weight=8.1 g) and purified over E. Merck silica gel 60 column in hexane/acetone mixtures to give 1.0 g of the monoacetate and 1.58 g of the diacetate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05242938uspto-grants-1993_09