Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224725Generated: October 31, 2026

Hydrochloric Acid → 4-(2,4-difluorophenyl)benzoic Acid

https://huagongshe.com/reaction/2224725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(2,4-difluorophenyl)benzoateHCID 57771752—
Solvent1,4-DioxaneHCID 31275—
Product4-(2,4-difluorophenyl)benzoic AcidHCID 275826424.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

Combine 4-carbomethoxyphenylboronic acid (1.021 g, 5.67 mmol), 1-bromo-2,4-difluorobenzene (1.000 g, 5.181 mmol.), Pd(OAc)2 (0.113 g, 0.50 mmol), triphenylphosphine (0.149 g, 0.505 mmol), and sodium carbonate (1.664 g, 0.568 mmol). Purge the reaction vessel with argon. Add DMF (20 mL) and water (2.0 mL) with stirring. Place sealed reaction in an 80° C. oil bath and allow to stir for 24 hours. 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 2′,4′-difluorobiphenyl-4-carboxylic acid methyl ester as a yellow solid. Dissolve the purified ester in dioxane (5 mL) and add 5M NaOH (1 mL). Stir vigorously at 50° C. for 15 hours. Upon completion, acidify the reaction with conc. HCl and extract with ethyl acetate. Evaporation of the solvent yields 300 mg (24.7%) of the title compound. MS (ES): m/z 233.0 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378447B2
Source datasetuspto-grants-2008_05
ORD IDord-d65b1d4b06194919b5b3896e87fa3217
Source noteuspto-grants-2008_05