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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454781Generated: October 30, 2026

Trifluoroacetic acid → HCID 58508822, compound

https://huagongshe.com/reaction/454781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58508948HCID 58508948—
ProductHCID 58508822HCID 58508822—

Reaction Steps

Trifluoroacetic acid (3.0 mL) was added to the obtained tert-butyl 4-anilino-2-(5-phenylpyridine-3-carboxamido)benzoate, followed by stirring at room temperature for 1 hour and 30 minutes. The solvent was evaporated under reduced pressure, and diisopropyl ether was added to the obtained residue. The solid substance was collected by filtration. Dioxane (3.0 mL) and a 2 mol/L aqueous solution of sodium hydroxide (0.068 mL) were sequentially added to the obtained solid substance, followed by stirring at room temperature for 1 hour and 30 minutes. A 10% aqueous solution of citric acid was added to the reaction mixture, and the solid substance was collected by filtration to obtain 73 mg of 4-anilino-2-(5-phenylpyridine-3-carboxamido)benzoic acid as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-bc852d24e6354233a4e9169c2a209692
Source noteuspto-grants-2013_07