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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285307Generated: October 26, 2026

Sodium Methoxide → 3-Methoxy-16-methyleneandrosta-3,5,9(11)-trien-17-one

https://huagongshe.com/reaction/1285307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant(8S,10R,13S,14S)-3-methoxy-10,13-dimethyl-1,2,7,8,12,14,15,16-octahydrocyclopenta[a]phenanthren-17-oneHCID 13037635—
SolventTetrahydrofuranHCID 8028—
Product3-Methoxy-16-methyleneandrosta-3,5,9(11)-trien-17-oneHCID 54551656—

Reaction Steps

3-Methoxyandrosta-3,5,9(11)-trien-17-one (IAa, 20 g) in THF (220 ml) was combined with dimethyloxylate (11.8 g) and sodium methoxide (25%, 18.4 ml) at 0° under nitrogen. After the reactants were combined, the ice was removed. After one hour, TLC shows the reaction has gone cleanly. Triethylamine (7.0 ml), acetic acid (1.0 ml), paraformaldehyde (3 g), and methanol (28 ml) were added and the mixture stirred overnight at 20°-25°. TLC showed the reaction had gone to completion. The reaction mixture was washed with phosphate buffer (121 ml) and water (202 ml). The mixture was extracted with methylene chloride (48 ml) and again with methylene chloride (40 ml). The methylene chloride extracts were combined and back-extracted with water (80 ml) and saline (10 ml). The organic mixture was concentrated under reduced presure to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04567001
Source datasetuspto-grants-1986_01
ORD IDord-a7f5072d3a524fca83247e4cbefa7ff3
Source noteuspto-grants-1986_01