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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255361Generated: October 25, 2026

4-Fluorophenol → 4-(4-Fluorophenoxy)-1,5-naphthyridine

https://huagongshe.com/reaction/2255361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
Reactant4-Chloro-1,5-naphthyridineHCID 596262—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product4-(4-Fluorophenoxy)-1,5-naphthyridineHCID 1973786947.1%

Reaction Steps

A mixture comprising 150 mg (0.911 mmole) of 4-chloro-1,5-naphthyridine and 1.00 g of 4-fluorophenol was heated at 160° C. After one hour, the mixture was cooled and dissolved in ethyl acetate and 2N sodium hydroxide. The organic layer was washed twice with base to remove excess 4-fluorophenol. The organic layer was then dried with magnesium sulfate and concentrated, producing an oil that slowly crystallized. This product was recrystallized in heptane, giving 103 mg of the title product. MP 122°-124° C. Yield 47%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240916
Source datasetuspto-grants-1993_08
ORD IDord-4a9ff2caa72f492a8f9c458e6cc984e4
Source noteuspto-grants-1993_08