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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803628Generated: October 25, 2026

Furan → 1-(Furan-2-yl)-2-(3-methoxyphenyl)ethan-1-one

https://huagongshe.com/reaction/1803628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant(3-Methoxyphenyl)acetic acidHCID 15719—
SolventDichloromethaneHCID 6344—
Product1-(Furan-2-yl)-2-(3-methoxyphenyl)ethan-1-oneHCID 6105687177%

Reaction Steps

3-Methoxyphenylacetic acid (20 g, 120.35 mmol) was dissolved in CH2Cl2 (200 mL), and furan (24.6 g, 361.39 mmol) and trifluoroacetic anhydride (37.8 g, 180 mmol) were added to the solution. The reaction was kept being stirred overnight at room temperature. The reaction was quenched with saturated NaHCO3 to pH=6.9, and the organic reagent in the mixture was evaporated. The residue was extracted with EtOAc, and the organic layer was washed with brine, dried over MgSO4, and evaporated. The resulting residue was purified by chromatography on a silica gel column using hexane-EtOAc as eluent to give 1-(furan-2-yl)-2-(3-methoxyphenyl)ethan-1-one as yellow oil: 20 g (yield: 77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-ff791bd6ebb94de0895cb9afd7536c6e
Source noteuspto-grants-2013_01