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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196316Generated: October 31, 2026

Hydrochloric Acid → 6alpha,7alpha-Diepoxypregn-4-en-3beta-ol

https://huagongshe.com/reaction/1196316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium borohydrideHCID 4311764—
Reactant6alpha,7alpha-Diepoxypregn-4-en-3oneHCID 86745798—
SolventWaterHCID 962—
Product6alpha,7alpha-Diepoxypregn-4-en-3beta-olHCID 8674579980%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.105 g (0.237 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3one and 6 ml of ethanol was added 9 mg (0.237 mmole) of sodium borohydride at a temperature of 0° C. and the mixture was stirred at 0° C. for 30 minutes. To the reaction mixture were added water and 1N-hydrochloric acid in the order mentioned and the mixture was extracted with methylene chloride. The aqueous layer was further extracted with methylene chloride and the extract was pooled with the previous methylene chloride extract. The mixture was washed successively with cold saturated sodium hydrogen carbonate solution and aqueous sodium chloride solution and the organic layer was dried over magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1:10, v/v) to recover 0.084 g of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3β-ol (yield: 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-f058d9a1e3184e91be295b0f34f88220
Source noteuspto-grants-1992_05