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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460479Generated: October 29, 2026

Hydrochloric Acid → 11-(3,17beta-Dihydroxyestra-1,3,5(10)-trien-11beta-yl)-2-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)undecanoic acid

https://huagongshe.com/reaction/460479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 11-(3,17beta-dihydroxyestra-1,3,5(10)-trien-11beta-yl)-2-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)undecanoateHCID 86588532—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product11-(3,17beta-Dihydroxyestra-1,3,5(10)-trien-11beta-yl)-2-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)undecanoic acidHCID 8658853384%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl 11-(3,17β-dihydroxyestra-1,3,5(10)-trien-11β-yl)-2-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)undecanoate (747 mg, 1.02 mmol) was dissolved in a mixed solvent of ethanol (5 ml) and water (5 ml). To this solution, NaOH (82 mg, 2.04 mmol) was added, and the resulting mixture was heated for 15 hours at 60° C. After cooling, 2N aqueous hydrochloric acid was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and then filtered. After concentration under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=4/1→3/1→2/1) to give 11-(3,17β-dihydroxyestra-1,3,5(10)-trien-11β-yl)-2-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)undecanoic acid (600 mg, Yield 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196081B2
Source datasetuspto-grants-2007_03
ORD IDord-f4bf8aa31fb2465896d7a33681de971a
Source noteuspto-grants-2007_03