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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 231239생성일: 2026년 10월 24일

Sulfuric Acid → HCID 13277552, 화합물

https://huagongshe.com/ko/reaction/231239

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물TetrahydrofuranHCID 8028—
반응물Sodium BicarbonateHCID 516892—
반응물(3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinoneHCID 53965319—
촉매Mercuric sulfateHCID 24544—
용매WaterHCID 962—
생성물HCID 13277552HCID 13277552—

반응 조건

온도25 °C

반응 단계

trans i.e. (3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone (0.08 g) is dissolved in a mixture of tetrahydrofuran (10 ml) and water (2 ml), and 0.02 g of mercury sulfate and a catalytic amount of concentrated sulfuric acid are added, followed by stirring at 25° C. for 3 hours. After addition of 0.1 g of sodium hydrogen carbonate, the mixture is concentrated to dryness under reduced pressure. The residue is extracted with 50 ml of ethyl acetate and the extract is concentrated to dryness. The residue is dissolved in 10 ml of ethyl acetate, and m-chloroperbenzoic acid (0.2 g) is added, followed by strirring for 50 hours. After addition of 0.2 ml of dimethyl sulfide, and the mixture is stirred further for 30 minutes and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography (eluent: 60% ethyl acetate-40% n-hexane) to give trans i.e. (3S,4R)-4-acetoxy-3-[(R)-1-hydroxyethyl]-2-azetidinone (0.04 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04845210
출처 데이터셋uspto-grants-1989_07
ORD IDord-14d9b31fc918400fa4ea5c428c04bca9
출처 메모uspto-grants-1989_07