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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582375Generated: October 26, 2026

Erythromycin → Erythromycin A enol ether

https://huagongshe.com/reaction/1582375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantErythromycinHCID 12560—
ReactantSodium BicarbonateHCID 516892—
SolventAcetic AcidHCID 176—
ProductErythromycin A enol etherHCID 8395463.6%

Reaction Steps

Glacial acetic acid solution of erythromycin A (12.4 g, 16.9 mmol) was stirred at room temperature for 2 hours, added slowly aqueous sodium hydrogen carbonate and neutralized. The reaction mixture was extracted with chloroform, dehydrated the organic layer with sodium sulfate, filtered off the sodium sulfate and removed the solvent by distillation to obtain crude substance. The crude substance was purified with silica gel chromatography (chloroform:methanol:aqueous ammonia=10:0.5:0.01→10:1:0.05) to obtain EM201 (7.7 g, 63%). Subsequently, potassium carbonate (1.4 g, 10.6 mmol) was added to the methanol solution (100 ml) of EM 201 (7.6 g, 10.6 mmol) and refluxed for 2 hours. After distilled off the solvent, the residue was dissolved in aqueous sodium hydrogen carbonate and extracted with chloroform. The mixture was dehydrated with sodium sulfate, filtered and removed the sodium sulfate, then the obtained crude substance was purified by silica gel chromatography (chloroform:methanol:aqueous ammonia=10:0.5:0.01→10:1:0.05) to obtain EM701 (5.9 g, 78%, white powder).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734292B1
Source datasetuspto-grants-2004_05
ORD IDord-89a604ed57824cd6b050648bd71b2039
Source noteuspto-grants-2004_05