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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409201Generated: October 28, 2026

4-Fluorophenol → 3-(4-Fluoro-phenoxy)-2-methyl-benzoic acid ethyl ester

https://huagongshe.com/reaction/409201

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantCesium carbonateHCID 10796—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
ReactantEthyl 3-iodo-2-methylbenzoateHCID 54051219—
CatalystCuprous chlorideHCID 62652—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-(4-Fluoro-phenoxy)-2-methyl-benzoic acid ethyl esterHCID 6711034254.5%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-iodo-2-methyl-benzoic acid ethyl ester (6.29 g, 0.02 mol), para-fluorophenol (4.86 g, 0.04 mol), cesium carbonate (14.14 g, 0.04 mol), 2,2,6,6-tetramethylheptane-3,5-dione (447 μL, 2 mmol) and copper (I) chloride (1.07 g, 0.01 mol) in anhydrous N-methyl-2-pyrrolidone (38 mL) was heated at 130° C. for 3 days before it was cooled to room temperature, quenched with water and filtered. The filtrate was extracted with ethyl acetate. The organic layer was washed twice with 0.5 N sodium hydroxide, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a pale green oil (2.99 g): 1H NMR (CDCl3, 200 MHz): δ=7.63 (m, 1H), 7.18 (m, 2H), 6.98 (m, 2H), 6.85 (m, 2H), 4.37 (q, J=7.0 Hz, 2H), 2.45 (s, 3H), 1.40 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759373B2
Source datasetuspto-grants-2014_06
ORD IDord-34b70b0315e245778a3815847620df1a
Source noteuspto-grants-2014_06