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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42110Generated: October 25, 2026

17,17-Bis(ethylendioxy)-5-androsten-7-one → 17,17-Bis(ethylendioxy)androstan-7-one

https://huagongshe.com/reaction/42110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17,17-Bis(ethylendioxy)-5-androsten-7-oneHCID 67537234—
Reactant3beta-Acetoxyandrostane-7,17-dioneHCID 69011313—
SolventEthyl AcetateHCID 8857—
Product17,17-Bis(ethylendioxy)androstan-7-oneHCID 6895071382%

Reaction Steps

17,17-Bis(ethylendioxy)androstane-7-one was prepared in 82% yield from 3,3:17,17-bis(ethylendioxy)-5-androsten-7-one by the procedure described above for the preparation of 3β-acetoxyandrostane-7,17-dione (Prepn. 29) using EtOAc instead of EtOH. The crude product was purified by flash chromatography (SiO2, n-hexane/EtOAc 6/4). 1H-NMR (300 MHz, acetone-d6, ppm from TMS: δ 3.96-3.75 (8H, m), 2.54-1.10 (20H, m), 1.13 (3H, s), 0.83 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536160B2
Source datasetuspto-grants-2013_09
ORD IDord-086cbeb82dba4328b163d8b3b7317183
Source noteuspto-grants-2013_09