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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66550Generated: October 30, 2026

Water → 21-Chloro-17alpha-hydroxy-20-methoxypregna-4,9(11),20-trien-3-one

https://huagongshe.com/reaction/66550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant21-Chloro-20-methoxy-21-(phenylsulfinyl)pregna-4,9(11),17(20)-trien-3-oneHCID 57012527—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product21-Chloro-17alpha-hydroxy-20-methoxypregna-4,9(11),20-trien-3-oneHCID 86738511—

Reaction Steps

To a solution of 21-chloro-20-methoxy-21-(phenylsulfinyl)pregna-4,9(11),17(20)-trien-3-one (VI, Example 3, 100 mg) in THF (2 ml), methanol (0.45 ml) and acetone (0.3 ml) at 0° under nitrogen is added a solution of sodium hydroxide (5 N, 0.04 ml). The mixture is brought to 20°-25° and is allowed to stir for 24 hr. The mixture is poured into a mixture of water (25 ml) and methylene chloride (10 ml). The layers are separated and the aqueous layer is extracted with methylene chloride (2×5 ml). The organic extracts are combined and washed with water (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04342702
Source datasetuspto-grants-1982_08
ORD IDord-4e98e46d8be14dc0b62c0c3aef402f49
Source noteuspto-grants-1982_08