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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727192Generated: October 26, 2026

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

https://huagongshe.com/reaction/1727192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclopentadieneHCID 6492—
ReactantMAGNESIUM SILICATE (synthetic)HCID 61680—
ReactantTrimethylamine oxide dihydrateHCID 198430—
ReactantSodium BisulfiteHCID 23665763—
CatalystOsmium TetroxideHCID 30318—
CatalystTetrabutylammonium AcetateHCID 82707—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product3a,4,5,6,7,7a-Hexahydro-1H-4,7-methanoindene-5,6-diolHCID 1316697619.6%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07494992B2
Source datasetuspto-grants-2009_02
ORD IDord-73906d6b0952423691dcef7cb06941fe
Source noteuspto-grants-2009_02