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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658708Generated: October 29, 2026

1,2-Dichloroethane → HCID 22791150, compound

https://huagongshe.com/reaction/1658708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactanttert-ButanolHCID 6386—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 22791146HCID 22791146—
SolventEthyl AcetateHCID 8857—
ProductHCID 22791150HCID 22791150—

Reaction Steps

750 mg. of 17α-ethinyl-11β-fluoro-17β-hydroxy-4,6-androstadien-3-one in 50 ml. of ethylene chloride is combined with 1.2 g. of m-chloroperbenzoic acid in 5 ml. of tert.-butanol and 1 ml. of ethylene chloride. The mixture is agitated at room temperature for 21 hours. The solution is then diluted with ethyl acetate and washed successively with sodium bisulfite solution and water. In this way, 420 mg. of 17α-ethinyl-6α,7α-epoxy-11β-fluoro-17β-hydroxy-4-androsten-3-one is isolated. UV: ε239 = 16,300 (methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966713
Source datasetuspto-grants-1976_06
ORD IDord-7d857957c39b4d298183026c13655e27
Source noteuspto-grants-1976_06