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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 464645Erstellt: 24. Oktober 2026

Acetone → 5,6-Dihydroxy-2-thiabicyclo[2.2.2]octan-3-one O-[(methylamino)carbonyl]oxime

https://huagongshe.com/de/reaction/464645

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetoneHCID 180—
EduktMagnesium orthosilicateHCID 66225—
EduktMethyl morpholine oxideHCID 82029—
EduktSodium BisulfiteHCID 23665763—
Edukt2-thiabicyclo[2.2.2]oct-5-en-3-one O-[(methylamino)carbonyl]oximeHCID 54323163—
KatalysatorOsmium TetroxideHCID 30318—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
Produkt5,6-Dihydroxy-2-thiabicyclo[2.2.2]octan-3-one O-[(methylamino)carbonyl]oximeHCID 54012477—

Reaktionsschritte

To a solution of 6.5 g (0.048 m) of N-methylmorpholine N-oxide and 5.0 g (0.024 m) of 2-thiabicyclo[2.2.2]oct-5-en-3-one O-[(methylamino)carbonyl]oxime in 20 ml of acetone was added 15 ml of a 0.5% solution of osmium tetroxide in tert-butanol. The reaction mixture was stirred at room temperature for 48 hours, then treated with a slurry of 1 g sodium bisulfite, 15 g of magnesium silicate, and 50 ml of water. After being stirred for 30 minutes, the mixture was filtered. The filtrate was extracted with ethyl acetate, then with methylene chloride. Evaporation of the dried organic solution gave 4.8 g of viscous oil. Purification by dry column chromatography yielded 3.5 g of the title compound as a white solid, m. 123°-5° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04548929
Quelldatensatzuspto-grants-1985_10
ORD IDord-6689a53c4f12421eb2d475620fde2eb4
Quellennotizuspto-grants-1985_10