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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848775Generated: October 30, 2026

2beta-Ethyl-17beta-methoxy-5alpha-androstan-3-one → 2alpha-Ethyl-17beta-methoxy-5alpha-androstan-3-one

https://huagongshe.com/reaction/848775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2beta-Ethyl-17beta-methoxy-5alpha-androstan-3-oneHCID 70562822—
CatalystSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
Product2alpha-Ethyl-17beta-methoxy-5alpha-androstan-3-oneHCID 12836849—

Reaction Steps

2β-Ethyl-17β-methoxy-5α-androstan-3-one (Step A) is dissolved in ethanol (95%, 13 ml.) followed by addition of sodium hydroxide (50%, 14 drops). After stirring at 20°-25° for 4.5 hrs. the mixture is extracted with diethyl ether, the diethyl ether extract is concentrated under reduced pressure to yield the title compound, which is recrystallized twice from methanol; m.p. 105°-107°; NMR (CDCl3) 0.77, 1.05, 3.20 and 3.33 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04297350
Source datasetuspto-grants-1981_10
ORD IDord-3363d3422175400f96ff40f04c7fae26
Source noteuspto-grants-1981_10