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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053694Generated: October 31, 2026

Hydrochloric Acid → 2-Fluoro-4-phenylbenzoic acid

https://huagongshe.com/reaction/2053694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-fluoro-4-phenylbenzoateHCID 69129634—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-4-phenylbenzoic acidHCID 1139029084%

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-5ac562ed753d48799069e9230ea9f11b
Source noteuspto-grants-2008_02