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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233640Generated: October 31, 2026

Hydrogen Peroxide → 3beta-(3-Hydroxypropoxy)-17beta-(3-furyl)-5beta-androstan-14beta-ol

https://huagongshe.com/reaction/233640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
Reactant9-Borabicyclo(3.3.1)nonaneHCID 78966—
Reactant3beta-Prop-2-enoxy-17beta(3-furyl)-5beta-androstan-14beta-olHCID 22854578—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3beta-(3-Hydroxypropoxy)-17beta-(3-furyl)-5beta-androstan-14beta-olHCID 70044091—

Reaction Steps

To a solution of 0.17 g of 9-borabicyclo[3.3.1]nonane in 35 ml of dry tetrahydrofuran, 0.50 g of 3β-(prop-2-enoxy)-17β-(3-furyl)-5β-androstan-14β-ol in 10 ml of tetrahydrofuran were added under nitrogen atmosphere, at room temperature. The solution was stirred for 6 hrs then 0.75 ml of ethanol, 0.25 ml of sodium hydroxide 6N and 0.50 ml of hydrogen peroxide 30% were added. The mixture was stirred at 50° C. for an hr, quenched with a solution of 0.76 g of potassium carbonate in 20 ml of water and the organic solvent distilled under reduced pressure. The residue was extracted with methylene chloride, the organic solution was dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure. The residue was purified by flash-chromatography (SiO2) using n-hexane/ethyl acetate 70/30 as eluant to give 0.40 g of 3β-(3-hydroxypropoxy)-17β-(3-furyl)-5β-androstan-14β-ol as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05593982
Source datasetuspto-grants-1997_01
ORD IDord-f35a8c067b554b15b811b1ef75b48b03
Source noteuspto-grants-1997_01