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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454615Generated: October 29, 2026

Trifluoroacetic acid → HCID 58508847, compound

https://huagongshe.com/reaction/454615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58508424HCID 58508424—
ProductHCID 58508847HCID 5850884785.1%

Reaction Steps

Trifluoroacetic acid (5.0 mL) was added to the obtained tert-butyl 2-(2-hydroxy-4-(piperidin-1-yl)benzamido)-4-phenylbenzoate (0.084 g), followed by stirring at room temperature for 4 hours. The solvent was evaporated under reduced pressure, and water and ethyl acetate were added to the residue, followed by adjusting the pH to 6.5 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. Diisopropyl ether was added to the obtained residue. The solid substance was collected by filtration to obtain 0.063 g of 2-(2-hydroxy-4-(piperidin-1-yl)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-9404899c4f204c1d9aae8406529b32ca
Source noteuspto-grants-2013_07