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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053693Generated: October 31, 2026

Cesium fluoride → Methyl 2-fluoro-4-phenylbenzoate

https://huagongshe.com/reaction/2053693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-2-fluoro-benzoic acid methyl esterHCID 11345311—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-fluoro-4-phenylbenzoateHCID 69129634—

Reaction Conditions

Temperature80 °C

Reaction Steps

Combine methyl 2-fluoro-4-bromobenzoate (1.25 g, 5.36 mmol), phenylboronic acid (1.30 g, 10.72 mmol) and CsF (2.02 g, 13.40 mmol) in DMF (25 mL) and water (3.0 mL) with stirring. Place the hetereogeneous reaction mixture open to the air in an oil bath maintained at 80° C. After 5 minutes of heating, add Pd(OAc)2 (120 mg, 0.536 mmol) in one portion and stir until reaction turns black. Cool reaction to room temperature, dilute with ethyl acetate and filter through a short plug of celite with additional ethyl acetate. Wash organics with water, dry over MgSO4, filter and evaporate. Purification by flash column chromatography yields 3-fluorobiphenyl-4-carboxylic acid methyl ester as a solid. Dissolve the purified ester in THF (0.25M) and add an equal volume of 1 M NaOH. Stir vigorously at room temperature for 15 hours. Upon completion, acidify the reaction with conc. HCl and extract with ethyl acetate. Evaporation of the solvent yields 965 mg (84%) of the title compound. MS (m/e): 214.9 (M−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326731B2
Source datasetuspto-grants-2008_02
ORD IDord-830f2c86c7b341fea80b114671a8c421
Source noteuspto-grants-2008_02