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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399967Generated: November 2, 2026

HCID 14304771, compound → HCID 70300251, compound

https://huagongshe.com/reaction/399967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14304771HCID 14304771—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70300251HCID 7030025123.1%

Reaction Steps

Under an argon atmosphere, a solution of potassium t-butoxide (4.13 g, 36.8 mmol) in dry tetrahydrofuran (500 ml) was cooled to -78° C., and a solution of 1α,3β-bis(t-butyldimethylsilyloxy)-17-oxoandrosta-5,7-diene (13.0 g, 24.5 mmol) in tetrahydrofuran (40 ml) was added dropwise. After the mixture was stirred at the same temperature for 1 hour, a solution of 2-(phenylsulfonyl)-3-phenyloxazyldine (9.62 g, 36.8 mmol) in tetrahydrofuran (40 ml) was added dropwise and the mixture was further stirred at -78° C. for 1.5 hour. The reaction mixture was quenched with an aqueous saturated ammonium chloride solution, poured into water and extracted with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The mixture was concentrated under reduced pressure and the deposited solids were filtered, then the filtrate was concentrated again and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate:chloroform=7:1:2) to give the title compound as a white solid (3.10 g, 23%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824811
Source datasetuspto-grants-1998_10
ORD IDord-a77630f7534e4147876b5d950526c1da
Source noteuspto-grants-1998_10