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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-phenyl-2-(5-phenylpyridine-2-carboxamido)benzoate | HCID 58508956 | — |
| Product | 4-Phenyl-2-(5-phenylpyridine-2-carboxamido)benzoic acid | HCID 58508621 | 93.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492582B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-d39c22690e5b44b8af59805e4242d073 |
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| Source note | uspto-grants-2013_07 |
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