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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080147Generated: October 29, 2026

4-Fluorophenol → 5-(4-Fluorophenoxy)furan-2-carbaldehyde

https://huagongshe.com/reaction/2080147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
Reactant5-NitrofurfuralHCID 12774—
ReactantSodium hydrideHCID 24758—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product5-(4-Fluorophenoxy)furan-2-carbaldehydeHCID 1104190698%

Reaction Steps

To a solution of 4-fluorophenol (2.39 g, 21.3 mmol) in dimethylsulfoxide (20 mL) was added sodium hydride (785 mg, 19.6-23.6 mmol, 60-72% in oil), and the solution was stirred at room temperature for 20 minutes. Next, a solution of 5-nitro-furan-2-carbaldehyde (3 g, 21.3 mmol) in dimethylsulfoxide (10 mL) was added dropwise, the solution was then stirred for 2 hours at room temperature. The reaction mixture was poured into brine, and the mixture was extracted with ethyl acetate. The fractionated organic layer was dried over anhydrous magnesium sulfate, then concentrated, and the title compound (4.3 g, 20.8 mmol, 98%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-9c8ca423efeb4d7e9a60dbcdb1fa6a88
Source noteuspto-grants-2011_04