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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454586Generated: October 26, 2026

Tert-butyl 2-(2-(benzyloxy)-5-(furan-3-yl)benzamido)-4-phenylbenzoate → Tert-butyl 2-(2-hydroxy-5-(tetrahydrofuran-3-yl)benzamido)-4-phenylbenzoate

https://huagongshe.com/reaction/454586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(2-(benzyloxy)-5-(furan-3-yl)benzamido)-4-phenylbenzoateHCID 66990487—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductTert-butyl 2-(2-hydroxy-5-(tetrahydrofuran-3-yl)benzamido)-4-phenylbenzoateHCID 5850889466.8%

Reaction Steps

To a solution mixture of tert-butyl 2-(2-(benzyloxy)-5-(furan-3-yl)benzamido)-4-phenylbenzoate (0.048 g) in methanol (2 mL) and dioxane (2 mL), 10% palladium-carbon (20 mg) was added, followed by stirring under a hydrogen atmosphere at room temperature for 2 hours. The insoluble substrate was removed by filtration, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography [Fuji Silysia Chemical Ltd., PSQ100B (spherical), eluent: 97-85% hexane/ethyl acetate] to obtain 0.027 g of tert-butyl 2-(2-hydroxy-5-(tetrahydrofuran-3-yl)benzamido)-4-phenylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-8ff7cb1b14634344b77e33a44fe96fb1
Source noteuspto-grants-2013_07