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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4988Erstellt: 23. Oktober 2026

Acetic Anhydride → Acetoacetic Acid

https://huagongshe.com/de/reaction/4988

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
EduktVirginiamycin M1HCID 5459319—
LösungsmittelPyridineHCID 1049—
ProduktAcetoacetic AcidHCID 96—
ProduktAcetateHCID 175—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05242938
Quelldatensatzuspto-grants-1993_09
ORD IDord-0d147c8237e642a6a930435c14340e40
Quellennotizuspto-grants-1993_09