Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803629Generated: November 2, 2026

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

https://huagongshe.com/reaction/1803629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant(3-Benzyloxyphenyl)acetic acidHCID 4592030—
SolventDichloromethaneHCID 6344—
Product1-(Furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-oneHCID 7117003595%

Reaction Steps

3-Benzyloxyphenylacetic acid (3.5 kg, 14.45 mol) was dissolved in CH2Cl2 (35 L), and furan (3.0 kg, 44 mol) and trifluoroacetic anhydride (4.55 kg, 21.65 mol) were added to the solution. The reaction was kept being stirred at room temperature for 2 days. 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 the 1-(furan-2-yl)-2-(3-benzyloxyphenyl)ethan-1-one as yellow oil: 4 kg (yield: 95%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350090B1
Source datasetuspto-grants-2013_01
ORD IDord-2ae8e23ad425433eb5add05167ade981
Source noteuspto-grants-2013_01