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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191685Generated: October 30, 2026

Ethanol → 4-(Benzylamino)-2-(4-fluoroanilino)benzoic acid

https://huagongshe.com/reaction/2191685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(benzylamino)-2-(4-fluoroanilino)benzoateHCID 57667993—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product4-(Benzylamino)-2-(4-fluoroanilino)benzoic acidHCID 5766809373.8%

Reaction Steps

10% Sodium hydroxide aqueous solution 0.82 mL was added to a suspension of ethanol 3.0 mL of methyl 4-(benzylamino)-2-(4-fluoroanilino)benzoate 0.24 g at room temperature, and it was heated and refluxed for 2 hours. After the reaction mixture was cooled to room temperature, 10% sodium hydroxide aqueous solution 0.82 mL was added, and it was heated and refluxed for 3 hours. After the reaction mixture was cooled to room temperature, acetic acid 2.0 mL, saturated sodium chloride aqueous solution 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. Diisopropyl ether and hexane were added to the obtained residue, and solid matter was filtrated to give 4-(benzylamino)-2-(4-fluoroanilino)benzoic acid 0.17 g of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-057cd676c6bc47dfa5e94caf7ac682e1
Source noteuspto-grants-2012_12