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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 231227Erstellt: 27. Oktober 2026

Sulfuric Acid → cis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone

https://huagongshe.com/reaction/231227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktSodium BicarbonateHCID 516892—
EduktWater ethylacetateHCID 22728543—
EduktCis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinoneHCID 57192380—
KatalysatorMercuric sulfateHCID 24544—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produktcis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinoneHCID 6778942918,1%

Reaktionsschritte

Cis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinone (0.24 g) is dissolved in a mixture of tetrahydrofuran (5 ml) and water (1 ml), and mercury sulfate (0.03 g) and concentrated sulfuric acid (0.06 g) are added, followed by stirring at room temperature for 15 hours. After addition of sodium hydrogen carbonate (0.2 g), the reaction mixture is poured into ethyl acetate-water, and the organic layer is separated, washed with aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography to give 0.03 g of cis-4-acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04845210
Quelldatensatzuspto-grants-1989_07
ORD IDord-cc66650d54a44bf4858200e34e1686f6
Quellennotizuspto-grants-1989_07