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HRID 1727192作成日:2026年10月27日

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

https://huagongshe.com/reaction/1727192

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclopentadieneHCID 6492—
反応物MAGNESIUM SILICATE (synthetic)HCID 61680—
反応物Trimethylamine oxide dihydrateHCID 198430—
反応物Sodium BisulfiteHCID 23665763—
触媒Osmium TetroxideHCID 30318—
触媒Tetrabutylammonium AcetateHCID 82707—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 1316697619.6%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07494992B2
出典データセットuspto-grants-2009_02
ORD IDord-73906d6b0952423691dcef7cb06941fe
出典メモuspto-grants-2009_02