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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454633Generated: October 27, 2026

Tert-butyl 2-(2-(benzyloxy)-5-phenoxybenzamido)-4-phenylbenzoate → Tert-butyl 2-(2-hydroxy-5-phenoxybenzamido)-4-phenylbenzoate

https://huagongshe.com/reaction/454633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(2-(benzyloxy)-5-phenoxybenzamido)-4-phenylbenzoateHCID 66991357—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(2-hydroxy-5-phenoxybenzamido)-4-phenylbenzoateHCID 5850859141.2%

Reaction Steps

To a solution mixture of the obtained tert-butyl 2-(2-(benzyloxy)-5-phenoxybenzamido)-4-phenylbenzoate (0.049 g) in methanol (1.5 mL) and ethyl acetate (1.5 mL), 10% palladium-carbon (0.025 g) was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours. To the reaction mixture, 10% palladium-carbon (0.050 g) was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours. Ethyl acetate was added to the reaction mixture, and the insoluble substance was removed by filtration. The solvent was evaporated under reduced pressure, and hexane was added to the obtained residue. The solid substance was collected by filtration to obtain 0.017 g of tert-butyl 2-(2-hydroxy-5-phenoxybenzamido)-4-phenylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-c7e8452651f447d68fc659f4ce599340
Source noteuspto-grants-2013_07