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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304206Generated: November 1, 2026

Hydrogen Peroxide → 1alpha,3beta-bis(tert-butyldimethylsilyloxy)-20(R)-(3-hydroxy-3-methylbutyloxy)pregna-5,7,16-triene

https://huagongshe.com/reaction/2304206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
ReactantLithium tri-s-butylborohydrideHCID 3611392—
Reactant1-bromo-2,3-epoxy-3-methylbutaneHCID 11041061—
Reactant1alpha,3beta-bis(tert-butyldimethylsilyloxy)-20(R)-hydroxypregna-5,7,16-trieneHCID 12020083—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product1alpha,3beta-bis(tert-butyldimethylsilyloxy)-20(R)-(3-hydroxy-3-methylbutyloxy)pregna-5,7,16-trieneHCID 1202008483%

Reaction Steps

A mixed solution of 1α,3β-bis(tert-butyldimethylsilyloxy)-20(R)-hydroxypregna-5,7,16-triene (51 mg, 0.0911 mmol), sodium hydride (50 mg, 2.08 mmol) and 4-bromo-2,3-epoxy-2-methylbutane (75 mg, 0.455 mmol) in tetrahydrofuran (2 ml) was heated under reflux for 1.5 hours and combined with 1M lithium tri-s-butylborohydride solution in tetrahydrofuran (0.9 ml, 0.900 mmol), and the mixed solution was heated under reflux for 20 minutes. The reaction solution was stirred with 3N aqueous sodium hydroxide solution and 30% aqueous hydrogen peroxide at room temperature for 30 minutes, then diluted with ethyl acetate, washed with brine and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by preparative thin layer chromatography (0.5 mm×1, hexane:ethyl acetate 10:1, developed twice) to give the title compound as a colorless oil (48.6 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06433200B1
Source datasetuspto-grants-2002_08
ORD IDord-a5e60550f0f64bd8a26ea3888e089d62
Source noteuspto-grants-2002_08