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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307536Generated: October 25, 2026

4-Fluorobenzyl chloride → 1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanone

https://huagongshe.com/reaction/2307536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzyl chlorideHCID 9602—
Reactant2-AcetylfuranHCID 14505—
CatalystZincchlorideHCID 3007855—
SolventWaterHCID 962—
Product1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanoneHCID 1013064074%

Reaction Conditions

Temperature85 °C

Reaction Steps

To 258 g (0.94 mol) of a 50% aqueous solution of zinc chloride were added 69.3 g of water, 99.0 g (0.90 mol) of 2-acetylfuran and 260 g (1.80 mol) of 4-fluorobenzylchloride. The mixture was stirred at 85° C. for 6 hours. The reaction mixture was cooled and extracted with ethylacetate. The extract was washed with 1N hydrochloric acid, washed with an aqueous sodium hydrogencarbonate solution and removed under reduced pressure. The obtained residue was distilled under reduced pressure to give 145.4 g of crude 2-acetyl-5-(4-fluorobenzyl)furan (106-121° C./0.4 mmHg). The crude product was recrystallized from isopropylalcohol/n-hexane to give 84.4 g of 2-acetyl-5-(4-fluorobenzyl)furan. Yield: 43%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831177B1
Source datasetuspto-grants-2004_12
ORD IDord-bf1d1dbb5ef84e9db47ec2295b75da8f
Source noteuspto-grants-2004_12