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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100473Generated: November 2, 2026

4-Fluorophenol → Ethyl 4-(4-fluorophenoxy)butanoate

https://huagongshe.com/reaction/2100473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantEthyl 4-chlorobutyrateHCID 18474—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductEthyl 4-(4-fluorophenoxy)butanoateHCID 560198—

Reaction Steps

Under cooling (0° C.), sodium ethanolate (2.18 g, 32 mmol) was added to a mixture of 4-fluorophenol ([371-41-5], 3.00 g, 27 mmol), ethyl 4-chlorobutyrate ([3153-36-4], 4.84 g, 32 mmol) and ethanol (15 ml), and the reaction mixture was then refluxed overnight. The solvent was evaporated, the residue was taken up in ethyl ester and was washed with water. After drying (Na2SO4), the solvent was evaporated, and 4-(4-fluoro-phenoxy)-butyric acid ethyl ester was isolated from the residue by column chromatography (silica gel, ethyl acetate/heptane). 1H NMR (d6-DMSO): 1.29 (t, 3H), 2.11 (tt, 2H), 2.51 (t, 2H), 3.96 (t, 2H), 4.13 (q, 2H), 6.79-6.85 (m, 2H), 6.92-6.99 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572801B2
Source datasetuspto-grants-2009_08
ORD IDord-4c880e51c4b647fcab12a7b0553f07bc
Source noteuspto-grants-2009_08