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HRID 464645作成日:2026年10月25日

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

https://huagongshe.com/reaction/464645

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Magnesium orthosilicateHCID 66225—
反応物Methyl morpholine oxideHCID 82029—
反応物Sodium BisulfiteHCID 23665763—
反応物2-thiabicyclo[2.2.2]oct-5-en-3-one O-[(methylamino)carbonyl]oximeHCID 54323163—
触媒Osmium TetroxideHCID 30318—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
生成物5,6-Dihydroxy-2-thiabicyclo[2.2.2]octan-3-one O-[(methylamino)carbonyl]oximeHCID 54012477—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04548929
出典データセットuspto-grants-1985_10
ORD IDord-6689a53c4f12421eb2d475620fde2eb4
出典メモuspto-grants-1985_10