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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467526Generated: October 29, 2026

Hydrochloric Acid → 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzoic acid

https://huagongshe.com/reaction/467526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrileHCID 51034749—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzoic acidHCID 67116046—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-(4-ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile (420 mg, 1.45 mmol; which may be prepared as described in D1) in methanol (15 mL) was added an aqueous solution of 6N NaOH (7.3 mL, 43.6 mmol). The reaction mixture was heated to reflux (70° C.) and stirred overnight. After cooling with an ice bath, concentrated HCl (3.7 mL) was added slowly. The mixture was diluted with ethyl acetate and water. The aqueous layer was separated and extracted twice with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtrated and concentrated in vacuo to give the title product as a beige solid (447 mg, quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623865B2
Source datasetuspto-grants-2014_01
ORD IDord-1491165ada964fb89cff1c0a6f394885
Source noteuspto-grants-2014_01