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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089424Generated: October 30, 2026

Ethyl vinyl ether → HCID 15085895, compound

https://huagongshe.com/reaction/1089424

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
ReactantHCID 15085894HCID 15085894—
ProductHCID 15085895HCID 15085895—

Reaction Steps

To a solution of 4 g of 4,4-difluoro-3β-(2-tetrahydropyranyloxy)androst-5-en-17β-ol in 50 ml of vinyl ethyl ether, there is added 0.25 g of mercuric acetate. The mixture is stirred at room temperature for 24 hours, quenched with triethylamine, and then poured into dilute aqueous potassium carbonate solution. The aqueous mixture is extracted three times with 100-ml portions of diethyl ether and the combined organic extracts are washed with saturated aqueous sodium chloride solution and then dried over sodium sulfate. The solvent is then removed under reduced pressure and the residue is purified by flash chromatography to give 4,4-difluoro-3β-(2-tetrahydropyranyloxy)-17β-ethenyloxyandrost-5-ene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966897
Source datasetuspto-grants-1990_10
ORD IDord-1c06a5f097b545b2ad929a05842f2be9
Source noteuspto-grants-1990_10