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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1727192생성일: 2026년 10월 26일

Dicyclopentadiene → 3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diol

https://huagongshe.com/reaction/1727192

반응식

참여 물질

역할이름HCID투입량
반응물DicyclopentadieneHCID 6492—
반응물MAGNESIUM SILICATE (synthetic)HCID 61680—
반응물Trimethylamine oxide dihydrateHCID 198430—
반응물Sodium BisulfiteHCID 23665763—
촉매Osmium TetroxideHCID 30318—
촉매Tetrabutylammonium AcetateHCID 82707—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 1316697619.6%

반응 단계

A slurry of tricyclo[5.2.1.02,6]deca-3,8-diene (26.5 g, 0.2 mol), trimethylamine N-oxide dihydrate (22.3 g, 0.2 mol) and osmium tetroxide (2.5 wt % solution in 2-methyl-2-propanol, 2 □l) in dichloromethane (200 ml) was stirred for 18 h. A further portion of osmium tetroxide (2.5 wt % solution in 2-methyl-2-propanol, ca. 2 □l) was added, water (25 ml) and acetone (50 ml) was added and the reaction mixture was stirred for a further 72 h. Pyridine (0.5 ml) and tetrabutylammonium acetate (0.5 g) were added. Florisil (10 g) and aqueous sodium hydrogensulfite solution was added and the reaction mixture was stirred for 20 min. The reaction mixture was filtered and the product was extracted with dichloromethane (3 times). The combined organic extracts were washed with water, brine and then concentrated to give an oil. The crude oil was purified by flash chromatography eluting with ethyl acetate:hexane (10:90) and then ethyl acetate, to give a waxy solid (6.5 g, 19%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07494992B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-73906d6b0952423691dcef7cb06941fe
출처 메모uspto-grants-2009_02