Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160674Generated: November 2, 2026

Water → 1-(3-Ethoxyphenyl)ethanone

https://huagongshe.com/reaction/1160674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
Reactant3-HydroxyacetophenoneHCID 8487—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-(3-Ethoxyphenyl)ethanoneHCID 3770250—

Reaction Conditions

Temperature70 °C

Reaction Steps

3′-Hydroxyacetophenone (200 mg) was dissolved in acetonitrile (4 ml). After adding ethyl iodide (0.2 ml) and potassium carbonate (347 mg), the mixture was stirred at 70° C. for 9 hours. After 9 hours, water and ethyl acetate were added to the reaction mixture followed by separation. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over sodium sulfate, filtered and concentrated. The crude product thus obtained was purified by silica gel chromatography (n-hexane:ethyl acetate=8:1) to thereby give 204 mg of 3′-ethoxyacetophenone. The procedure employed for the synthesis of F-12 was repeated but replacing the 3′-methoxyacetophenone by 3′-ethoxyacetophenone to thereby give (±)-N-(1-(3-ethoxyphenyl)ethyl)-2-(2′,5′-dichlorophenylthio)ethylamine (F-63). MS m/z: 369 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816408B2
Source datasetuspto-grants-2010_10
ORD IDord-bb8e94b096a54bada8769b4fa4971c6e
Source noteuspto-grants-2010_10