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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5338Generated: October 28, 2026

Tetrabutylammonium Fluoride → 11beta-(4-Acetylphenyl)-17alpha-hydroxy-17-(2-propinyl)14beta-estra-4,9-dien-3-one

https://huagongshe.com/reaction/5338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant11beta-(4-Acetylphenyl)-17alpha-hydroxy-17-(3-trimethysilyl-2-propinyl)-14beta-estra-4,9-dien-3-oneHCID 14623400—
SolventTetrahydrofuranHCID 8028—
Product11beta-(4-Acetylphenyl)-17alpha-hydroxy-17-(2-propinyl)14beta-estra-4,9-dien-3-oneHCID 1462340269.6%

Reaction Steps

470 mg of 11beta-(4-Acetylphenyl)-17alpha-hydroxy-17-(3-trimethysilyl-2-propinyl)-14beta-estra-4,9-dien-3-one in 24 ml of tetrahydrofuran is mixed with 2.35 ml of a 1M solution of tetrabutylammonium fluoride in tetrahydrofuran and stirred for 5 minutes at room temperature. It is poured on water and extracted with ethyl acetate. The combined organic phases are washed with water, dried on sodium sulfate and concentrated by evaporation. The residue is chromatographed with a mixture of hexane/ethyl acetate on silica gel. 280 mg of the title compound is isolated as foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244886
Source datasetuspto-grants-1993_09
ORD IDord-5496bc558f464336aaaccae32ef16785
Source noteuspto-grants-1993_09