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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440971Generated: October 30, 2026

Potassium Carbonate → HCID 53882777, compound

https://huagongshe.com/reaction/1440971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHydrofluoric AcidHCID 14917—
ReactantHCID 22859494HCID 22859494—
ReactantHydrogen fluoride tetrahydrofuranHCID 69735124—
ReactantHCID 178435160HCID 178435160—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53882777HCID 5388277770%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of anhydrous hydrogen fluoride (6 g) in tetrahydrofuran (11.8 g) and chloroform (6 ml) contained in a screw-capped polyethylene bottle chilled to about -60° C. was added a solution of 4-acetamino-1,2α-epoxy-androsta-4,6-diene-3,17-dione (3.554 g, 10 mmol) in chloroform (30 ml) likewise chilled to about -60° C. The hydrogen fluoride-tetrahydrofuran reagent was immersed in an acetone-dry ice bath while the steroid was being added. Additional chloroform (6 ml) was used to aid the transfer of the epoxide. Subsequently the reaction mixture was maintained at -30° C. for 4 h and then added gradually to a well agitated mixture of an aqueous solution of potassium carbonate, chloroform and ice. The organic layer was separated, the alkaline aqueous layer back-extracted twice with chloroform and the combined organic layers were evaporated to dryness. The residue was submitted to flash chromatography with ethyl acetate-ethanol to give pure 4-acetylamino-2-fluoroandrosta-1,4,6-triene-3,17-dione in 70% yield (2.502 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502044
Source datasetuspto-grants-1996_03
ORD IDord-ae685ad406ba415f868d88549dfe3abf
Source noteuspto-grants-1996_03