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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454594Generated: October 30, 2026

Trifluoroacetic acid → HCID 58508575, compound

https://huagongshe.com/reaction/454594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58508615HCID 58508615—
ProductHCID 58508575HCID 5850857559.9%

Reaction Steps

Trifluoroacetic acid (5 mL) was added to the obtained tert-butyl 2-(2-hydroxy-4-(methylamino)benzamido)-4-phenylbenzoate (0.027 g), followed by stirring at room temperature for 3 hours. The solvent was evaporated under reduced pressure, and water and ethyl acetate were added to the residue, followed by adjusting the pH to 6 with a saturated aqueous solution of sodium bicarbonate. The organic layer was separated, washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Hexane and diisopropyl ether were added to the obtained residue, and the solid substance was collected by filtration to obtain 0.014 g of 2-(2-hydroxy-4-(methylamino)benzamido)-4-phenylbenzoic acid as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-87f3678177b84537b43bfb48c077e768
Source noteuspto-grants-2013_07