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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454767Generated: October 30, 2026

Trifluoroacetic acid → 4-Phenyl-2-(5-phenylpyridine-2-carboxamido)benzoic acid

https://huagongshe.com/reaction/454767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-phenyl-2-(5-phenylpyridine-2-carboxamido)benzoateHCID 58508956—
Product4-Phenyl-2-(5-phenylpyridine-2-carboxamido)benzoic acidHCID 5850862193.5%

Reaction Steps

Trifluoroacetic acid (5 mL) was added to the obtained tert-butyl 4-phenyl-2-(5-phenylpyridine-2-carboxamido)benzoate (0.11 g), followed by stirring at room temperature for 4 hours. The solvent was evaporated under reduced pressure, and ethyl acetate and water were added to the obtained residue. After adjusting the pH to 6.5 with a saturated aqueous solution of sodium bicarbonate, the organic layer was separated, washed with water and a saturated aqueous solution of sodium chloride sequentially, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue, and the solid substance was collected by filtration to obtain 90 mg of 4-phenyl-2-(5-phenylpyridine-2-carboxamido)benzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-d39c22690e5b44b8af59805e4242d073
Source noteuspto-grants-2013_07