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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295291Generated: October 26, 2026

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

https://huagongshe.com/reaction/2295291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMagnesium orthosilicateHCID 66225—
ReactantMethyl morpholine oxideHCID 82029—
ReactantSodium BisulfiteHCID 23665763—
Reactant2-thiabicyclo[2.2.2]oct-5-en-3-one O-[(methylamino)carbonyl]oximeHCID 54323163—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product5,6-Dihydroxy-2-thiabicyclo[2.2.2]octan-3-one O-[(methylamino)carbonyl]oximeHCID 54012477—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04424213
Source datasetuspto-grants-1984_01
ORD IDord-0f027d10c8fc40e7ad6cfca59e58188b
Source noteuspto-grants-1984_01