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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454540Generated: October 29, 2026

Acetic Acid → HCID 58508898, compound

https://huagongshe.com/reaction/454540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 66990202HCID 66990202—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58508898HCID 5850889867.8%

Reaction Steps

To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-5-(pyridin-3-yl)benzamido)-4-phenylbenzoate (0.14 g) in ethyl acetate (1 mL) and methanol (1 mL), 10% palladium-carbon (14 mg) was added, followed by stirring under a hydrogen atmosphere at room temperature for 1 hour and 30 minutes. To the reaction mixture, 10% palladium-carbon (14 mg) was added. The resulting mixture was stirred under a hydrogen atmosphere at room temperature for 2 hours and 30 minutes. Acetic acid (2 mL) and 10% palladium-carbon (0.11 g) were added to the reaction mixture, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours. The insoluble substance was removed by filtration, and the solvent was evaporated under reduced pressure. Ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added to the residue. The organic layer was separated, washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride sequentially, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Trifluoroacetic acid (5 mL) was added to the obtained residue, followed by stirring at room temperature for 5 hours. The solvent was evaporated under reduced pressure, and water and ethyl acetate were added to the residue. After adjusting the pH to 5 with a saturated aqueous solution of sodium bicarbonate, the solid substance was collected by filtration to obtain 0.070 g of 2-(2-hydroxy-5-(pyridin-3-yl)benzamido)-4-phenylbenzoic acid as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-40fb606cb4c74a708ebc7b43845fa864
Source noteuspto-grants-2013_07