تفاعل #5083

ord-acac8f88fae84d0d92a648b8d5b90be2

الكواشف

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المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىfollowed by flash evaporation to dryness at room temperature
  2. 2
    أخرىThe residue was partitioned between dichloromethane (3×300 ml) and saturated NaCl (aq, 300 ml)
  3. 3
    تجفيفdried over anhydrous Na2SO4, flash
  4. 4
    أخرىevaporated to dryness (dry weight=8.1 g)
  5. 5
    أخرىpurified over E

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242938uspto-grants-1993_09