돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 464645생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Magnesium orthosilicateHCID 66225—
반응물Methyl morpholine oxideHCID 82029—
반응물Sodium BisulfiteHCID 23665763—
반응물2-thiabicyclo[2.2.2]oct-5-en-3-one O-[(methylamino)carbonyl]oximeHCID 54323163—
촉매Osmium TetroxideHCID 30318—
용매WaterHCID 962—
용매tert-ButanolHCID 6386—
생성물5,6-Dihydroxy-2-thiabicyclo[2.2.2]octan-3-one O-[(methylamino)carbonyl]oximeHCID 54012477—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04548929
출처 데이터셋uspto-grants-1985_10
ORD IDord-6689a53c4f12421eb2d475620fde2eb4
출처 메모uspto-grants-1985_10