HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440971Generated: October 30, 2026
Potassium Carbonate → HCID 53882777, compound
https://huagongshe.com/reaction/1440971
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Reactant | HCID 22859494 | HCID 22859494 | — |
| Reactant | Hydrogen fluoride tetrahydrofuran | HCID 69735124 | — |
| Reactant | HCID 178435160 | HCID 178435160 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53882777 | HCID 53882777 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05502044 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-ae685ad406ba415f868d88549dfe3abf |
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| Source note | uspto-grants-1996_03 |
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