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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 48957Generated: October 26, 2026

Dehydroepiandrosterone → Dehydroepiandrosterone

https://huagongshe.com/reaction/48957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDehydroepiandrosteroneHCID 5881—
Reactant22,29-EPOXY-3,29-DIHYDROXY-14beta-STIGMASTAN-15-ONEHCID 69625815—
ProductDehydroepiandrosteroneHCID 5881—
ProductHCID 178420941HCID 178420941—

Reaction Steps

The synthesis of 22,29-epoxy-3,29-dihydroxy-14β-stigmastan-15-one (260) can be accomplished in ten steps from dehydroisoandrosterone (247). Catalytic hydrogenation of the Δ5 carbon-carbon double bond in compound 247 yields compound 250, which contains a trans-fused A/B ring-system. Compound 247 is dissolved in EtOAc and 10% Pd/C is added. The mixture is stirred under H2 at room temperature overnight. Filtration through celite and concentration yields compound 250, which can be used directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706701B1
Source datasetuspto-grants-2004_03
ORD IDord-d863766c08014899a9c4dffcca1796e9
Source noteuspto-grants-2004_03