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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385617Generated: November 2, 2026

Hydrochloric Acid → (3beta,20S)-pregn-5-ene-3,20-diol 20-acetate

https://huagongshe.com/reaction/1385617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant(3beta,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol acetateHCID 57200658—
SolventAcetoneHCID 180—
Product(3beta,20S)-pregn-5-ene-3,20-diol 20-acetateHCID 2196930397.1%

Reaction Steps

iv)—A solution of (3β,20S)-3-[(1-ethoxyethyl)oxy]pregn-5-en-20-ol acetate (66.1 g) in acetone (1330 ml) was treated with a 4 M aqueous solution of hydrochloric acid (13.2 ml). The reaction mixture was stirred for 45 min. and subsequently poured into a mixture of water (3 l) and a saturated aqueous solution of sodium hydrogen carbonate (500 ml). The resulting precipitate was collected by filtration and then dissolved in dichloromethane. The filtrate was extracted with ethyl acetate. The dichloromethane and ethyl acetate solutions were washed with a saturated aqueous solution of sodium hydrogen carbonate and with brine, dried over sodium sulfate, and concentrated under reduced pressure to give (3β,20S)-pregn-5-ene-3,20-diol 20-acetate (compound 5; 53.5 g), which was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262282B1
Source datasetuspto-grants-2001_07
ORD IDord-1d49ac941c634e80a46e7f4ac6bbd478
Source noteuspto-grants-2001_07