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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792225Generated: November 3, 2026

Tetrahydrofuran → HCID 86760158, compound

https://huagongshe.com/reaction/1792225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86589971HCID 86589971—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 86760158HCID 8676015880.1%

Reaction Steps

To 1α,3β-bis(tert-butyldimethylsilyloxy)-17β-(N,N-dimethylaminocarbonylethoxymethyl)androsta-5,7-diene 4-phenyl-1,2,4-triazoline-3,5-dione adduct (9 g), were added tetrahydrofuran (90 ml) and then potassium t-butoxide (10.5 g), followed by reaction at room temperature for 10 min. After stopping the reaction by adding saturated brine, the reaction mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, evaporated under reduced pressure to remove the solvent and the thus obtained residue was purified by column chromatography (hexane:ethyl acetate=2:1) to give the titled compound (6.34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074777B2
Source datasetuspto-grants-2006_07
ORD IDord-5385123b715d4c92b06b49dff910a28e
Source noteuspto-grants-2006_07