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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293218Generated: October 30, 2026

4-Fluorophenol → Methyl 5-chloro-2-(4-fluorophenoxy)benzoate

https://huagongshe.com/reaction/1293218

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 5-chloro-2-fluorobenzoateHCID 21525433—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-chloro-2-(4-fluorophenoxy)benzoateHCID 5757228565%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred solution of 4-fluorophenol (1.60 g, 14.3 mmol) and sodium hydride (0.34 g, 14.3 mmol) in N,N-dimethylforamide (30 mL) was added a solution of methyl 5-chloro-2-fluorobenzoate (2.70 g, 14.3 mmol) in N,N-dimethylforamide (30 mL) at 0° C. The resulting mixture was heated at 120° C. for 16 h. After cooling to room temperature, the mixture was diluted with ether (300 mL) and washed with water (150 mL×3). The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by flush column chromatography on silica gel eluting with hexane/ethyl acetate (20:1) to afford 2.60 g (65%) of the title compounds as slight yellow oil: 1H-NMR (CDCl3) δ 7.88 (1H, d, J=2.8 Hz), 7.40 (1H, dd, J=8.8, 2.8 Hz), 7.06–6.85 (5H, m), 3.84 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238714B2
Source datasetuspto-grants-2007_07
ORD IDord-448d7668b5944fa19368808e06f24727
Source noteuspto-grants-2007_07