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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1196213생성일: 2026년 10월 23일

Boron trifluoride etherate → (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone

https://huagongshe.com/ko/reaction/1196213

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물1,3-DimethoxybenzeneHCID 9025—
반응물(3S,4R)-4-(1-(R)-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinoneHCID 67798445—
용매DichloromethaneHCID 6344—
생성물(3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinoneHCID 13960427—

반응 단계

To a solution of (3S,4R)-4-(1-(R)-t-butyldimethylsilyloxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (20 g) in dry dichloromethane (200 ml) were added 1,3-dimethoxybenzene (7.8 g) and boron trifluoride etherate (23 g) at 10 °-20° C., and the resultant mixture was stirred at room temperature for 3 hours, followed by heating under reflux for 3-5 hours. The reaction mixture was cooled down to 10°-15° C., washed successively with brine (200 ml×2), 2.5% sodium bicarbonate (200 ml) and brine (200 ml) and dried over anhydrous sodium sulfate. Filtration and concentration of the filtrate in vacuo gave an oily residue which was purified by silica gel chromatography to yield (3S,4S)-4-(1-(R)-hydroxymethylethyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05112966
출처 데이터셋uspto-grants-1992_05
ORD IDord-ca7f59f82f7343c2823d7361a964354d
출처 메모uspto-grants-1992_05