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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606488Generated: November 2, 2026

Triethylamine → 20,20-Ethylenedioxy-3alpha-hydroxy-2alpha-methyl-5alpha-pregnane-11-one

https://huagongshe.com/reaction/1606488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethyl phosphiteHCID 8472—
Reactant20,20-Ethylenedioxy-2beta-methyl-5alpha-pregnane-3,11-dioneHCID 86733332—
CatalystTetrachloroiridium--hydrogen chloride--water (1/2/1)HCID 16211483—
SolventIsopropanolHCID 3776—
Product20,20-Ethylenedioxy-3alpha-hydroxy-2alpha-methyl-5alpha-pregnane-11-oneHCID 7058512763.3%

Reaction Steps

A solution of chloroiridic acid (10 mg.) and trimethyl phosphite (1.5 ml.) in aqueous 90% isopropanol (20 ml.) was heated under reflux for 17 hours. The solution was then neutralised with triethylamine, 20,20-ethylenedioxy-2β-methyl-5α-pregnane-3,11-dione (0.66 g.) was added, and the mixture was heated under reflux for 48 hr. The reaction mixture was cooled and partitioned between methylene chloride and water. The organic layer was dried (MgSO4) and evaporated in vacuo. The residue (0.69 g.) was purified by preparative layer chromatography and crystallised from methyl acetate/petroleum ether (b.p. 60°-80°) to give 20,20-ethylenedioxy-3α-hydroxy-2α-methyl-5α-pregnan-11-one (0.42 g.), m.p. 167°-168°, [α]D + 68°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953429
Source datasetuspto-grants-1976_04
ORD IDord-390ef995a30c4c33a80453265931943e
Source noteuspto-grants-1976_04