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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606487Generated: October 31, 2026

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

https://huagongshe.com/reaction/1606487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethyl phosphiteHCID 8472—
Reactant20,20-Ethylenedioxy 2-hydroxymethylene-5alpha-pregnane-3,11-dioneHCID 86733331—
CatalystTetrachloroiridium--hydrogen chloride--water (1/2/1)HCID 16211483—
SolventIsopropanolHCID 3776—
Product20,20-Ethylenedioxy-2alpha-methyl-5alpha-pregnane-3,11-dioneHCID 867333306.7%

Reaction Steps

A solution of chloroiridic acid (30 mg.) and trimethyl phosphite (4.5 ml.) in aqueous 90% isopropanol (60 ml.) was heated under reflux for 17 hr. The solution was then neutralised with triethylamine and 20,20-ethylenedioxy 2-hydroxymethylene-5α-pregnane-3,11-dione (2 g.) was added. The mixture was heated under reflux for 40 hr. then cooled and partitioned between water and methylene chloride. The organic layer was dried (MgSO4) and evaporated in vacuo. The residue (1.94 g.) was subjected to preparative t.l.c. giving two fractions. The less polar fraction (0.18 g.) was crystallised from methanol to give 20,20-ethylenedioxy-2α-methyl-5α-pregnane-3,11-dione (0.13 g.), m.p. 179°-180°, [α]D + 77.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953429
Source datasetuspto-grants-1976_04
ORD IDord-697ca9dfd62f4d70aedfd9132700c478
Source noteuspto-grants-1976_04