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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4987Generated: October 26, 2026

Acetic Anhydride → Acetoacetic Acid

https://huagongshe.com/reaction/4987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantVirginiamycin M1HCID 5459319—
SolventPyridineHCID 1049—
ProductAcetoacetic AcidHCID 96—
ProductAcetateHCID 175—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242938
Source datasetuspto-grants-1993_09
ORD IDord-acac8f88fae84d0d92a648b8d5b90be2
Source noteuspto-grants-1993_09