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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191666Generated: November 2, 2026

Hydrochloric Acid → 4-(Cyclohexyloxy)-2-(4-fluoroanilino)benzoic acid

https://huagongshe.com/reaction/2191666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsopropanolHCID 3776—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 4-(cyclohexyloxy)-2-(4-fluoroanilino)benzoateHCID 57668066—
SolventEthyl AcetateHCID 8857—
Product4-(Cyclohexyloxy)-2-(4-fluoroanilino)benzoic acidHCID 5766800220.9%

Reaction Steps

10% Sodium hydroxide aqueous solution 0.25 mL was added to a suspension of 2-propanol 2.0 mL of methyl 4-(cyclohexyloxy)-2-(4-fluoroanilino)benzoate 40 mg at room temperature, and it was heated and refluxed for 5 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. Diisopropyl ether and hexane were added to the obtained residue, and solid matter was filtrated to give 4-(cyclohexyloxy)-2-(4-fluoroanilino)benzoic acid 8 mg of white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08327467B2
Source datasetuspto-grants-2012_12
ORD IDord-0ee9a5cb7b074377be538df55908c6e4
Source noteuspto-grants-2012_12