Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912667Generated: November 1, 2026

3beta-Hydroxy-5alpha,6alpha-epoxyandrostane-17-one → HCID 86651494, compound

https://huagongshe.com/reaction/1912667

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3beta-Hydroxy-5alpha,6alpha-epoxyandrostane-17-oneHCID 7075155—
ReactantHCID 86651495HCID 86651495—
ProductHCID 86651494HCID 8665149445%

Reaction Steps

17,17-Bis(ethylendioxy)-5α,6α-epoxyandrostane was prepared in 45% yield from 3,3:17,17-bis(ethylendioxy)-5-androstene by the procedure described above for the preparation of 3β-hydroxy-5α,6α-epoxyandrostan-17-one (Prepn. 4). The crude product was purified by flash chromatography (SiO2, n-hexane/EtOAc 80/20). 1H-NMR (300 MHz, acetone-d6, ppm from TMS): δ 3.92-3.75 (m, 8H), 2.68 (m, 1H), 2.56 (d, 1H), 1.99-1.06 (m, 18H), 1.09 (s, 3H), 0.78 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609644B2
Source datasetuspto-grants-2013_12
ORD IDord-b3b83fd6236e42e2952abc4602da9821
Source noteuspto-grants-2013_12