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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231239Erstellt: 24. Oktober 2026

Sulfuric Acid → HCID 13277552, Verbindung

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTetrahydrofuranHCID 8028—
EduktSodium BicarbonateHCID 516892—
Edukt(3S,4S)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinoneHCID 53965319—
KatalysatorMercuric sulfateHCID 24544—
LösungsmittelWaterHCID 962—
ProduktHCID 13277552HCID 13277552—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845210
Quelldatensatzuspto-grants-1989_07
ORD IDord-14d9b31fc918400fa4ea5c428c04bca9
Quellennotizuspto-grants-1989_07