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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454668Generated: October 30, 2026

HCID 66990889, compound → HCID 58508522, compound

https://huagongshe.com/reaction/454668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66990889HCID 66990889—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 58508522HCID 5850852224.5%

Reaction Steps

To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-4-(2-(morpholin-4-yl)ethoxy)benzamido)-4-phenylbenzoate (0.059 g) in methanol (2.0 mL) and ethyl acetate (2.0 mL), 10% palladium-carbon (0.012 g) was added, followed by stirring under a hydrogen atmosphere at room temperature for 3 hours. The insoluble substance was removed by filtration, and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue, and the solid substance was collected by filtration. Trifluoroacetic acid (4.0 mL) was added to the obtained solid substance, followed by stirring at room temperature for 3 hours. Toluene was added to the reaction mixture, and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue, and the solid substance was collected by filtration. Ethanol (4.0 mL) was added to the obtained solid substance. After adjusting the pH to 7.7 with a 1 mol/L aqueous solution of sodium hydroxide, the solid substance was collected by filtration to obtain 0.011 g of 2-(2-hydroxy-4-(2-(morpholin-4-yl)ethoxy)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-a1d4b476d2d24193bc63d38ebe503610
Source noteuspto-grants-2013_07