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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1582375생성일: 2026년 10월 27일

Erythromycin → Erythromycin A enol ether

https://huagongshe.com/reaction/1582375

반응식

참여 물질

역할이름HCID투입량
반응물ErythromycinHCID 12560—
반응물Sodium BicarbonateHCID 516892—
용매Acetic AcidHCID 176—
생성물Erythromycin A enol etherHCID 8395463.6%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06734292B1
출처 데이터셋uspto-grants-2004_05
ORD IDord-89a604ed57824cd6b050648bd71b2039
출처 메모uspto-grants-2004_05