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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973724Generated: November 2, 2026

Water → 20-Ethoxy-21-formyl-3alpha-hydroxy-5alpha-pregn-20-en-11-one

https://huagongshe.com/reaction/1973724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium BicarbonateHCID 516893—
Reactant3alpha-Acetoxy-20-ethoxy-21-formyl-5alpha-pregn-20-en-11-oneHCID 86734291—
SolventEthanolHCID 702—
Product20-Ethoxy-21-formyl-3alpha-hydroxy-5alpha-pregn-20-en-11-oneHCID 8673429034.1%

Reaction Steps

A solution of 3α-acetoxy-20-ethoxy-21-formyl-5α-pregn-20-en-11-one (500 mg) in ethyl alcohol (15 ml) was treated with potassium bicarbonate (450 mg) and the mixture was refluxed, under nitrogen, for 7 hours, then poured into water. The product was extracted with methylene chloride, and the extract washed with water, dried and evaporated. Purification of the residue (37 mg) by preparative t.l.c. and crystallisation from methyl acetate/petrol gave title compound (154 mg) m.p. 175°-178°, [α]D - 115.9°, λmax. 258 nm (ε 18,780).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998829
Source datasetuspto-grants-1976_12
ORD IDord-f65945e4ee004e68b5a645f3d27a022e
Source noteuspto-grants-1976_12