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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847189Generated: October 31, 2026

Hydrochloric Acid → 2-(4-Fluorophenoxy)benzoic acid

https://huagongshe.com/reaction/847189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Iodobenzoic acidHCID 6941—
ReactantNitrobenzeneHCID 7416—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product2-(4-Fluorophenoxy)benzoic acidHCID 3008367—

Reaction Conditions

Temperature160 °C

Reaction Steps

To 147 g of iodobenzoic acid and 45.5 g of potassium carbonate are added 57 ml of nitrobenzene. The mixture is heated with stirring at 160° C. for 40 minutes. To the heated mixture is added an additional 46.5 g of potassium carbonate and then successively 73.1 g of 4-fluorophenol, another 46.5 g of potassium carbonate and 0.3 g of copper powder. After these additions, the mixture is stirred at 160° C. for 45 minutes and the resulting solid is cooled to 0° C. The cooled solid is mixed with 100 ml of water and 220 ml of 6N hydrochloric acid. The acidic mixture is diluted with water to a volume of one liter and then mixed with 450 ml of chloroform. The white solid is filtered off and washed with chloroform and water. The solid is dissolved in hot acetone, cooled and filtered to leave a white crystalline product, mp 146°-147° C. of 2-(4-fluorophenoxy)benzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140027
Source datasetuspto-grants-1992_08
ORD IDord-e377be9a7c12464e92a71c7f4e77c04a
Source noteuspto-grants-1992_08