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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191695Generated: November 1, 2026

Hydrochloric Acid → 2-(4-Fluoroanilino)-4-(3-phenylpropyl)benzoic acid

https://huagongshe.com/reaction/2191695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(4-fluoroanilino)-4-(3-phenylpropyl)benzoateHCID 57668036—
SolventEthyl AcetateHCID 8857—
Product2-(4-Fluoroanilino)-4-(3-phenylpropyl)benzoic acidHCID 5766780672.8%

Reaction Steps

10% Sodium hydroxide aqueous solution 0.2 mL was added to a suspension of ethanol 2.0 mL of methyl 2-(4-fluoroanilino)-4-(3-phenylpropyl)benzoate 0.10 g at room temperature, and it was heated and refluxed for 2 hours. After the reaction mixture was cooled to room temperature, 1.0 mol/L hydrochloric acid and ethyl acetate were added to it. The organic layer was separated and collected,dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. Hexane was added to the obtained residue, and solid matter was filtrated to give 2-(4-fluoroanilino)-4-(3-phenylpropyl)benzoic acid 70 mg of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-836c67c015324e0c95f4331d2f132c96
Source noteuspto-grants-2012_12