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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700254Generated: November 2, 2026

Estrone → Estrone-3-oxylacetic acid

https://huagongshe.com/reaction/1700254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEstroneHCID 5870—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductEstrone-3-oxylacetic acidHCID 22528937.5%

Reaction Steps

The mixture of estrone (540 mg, 2.0 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol), and acetone (25 ml) was refluxed for 6 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 2, and then extracted three times with ethyl acetate (15 ml each). The organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethanol to give 246 mg estra-1,3,5(10)-trien-17-one-3-oxyacetic acid as white crystals, mp 205-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350756B1
Source datasetuspto-grants-2002_02
ORD IDord-87c883fea3f44b0783685a5683473ba0
Source noteuspto-grants-2002_02