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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454590Generated: October 30, 2026

Ethyl Acetate → HCID 66990706, compound

https://huagongshe.com/reaction/454590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66990211HCID 66990211—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 66990706HCID 6699070649.2%

Reaction Steps

Iron powder (43 mg) was added to a solution mixture of tert-butyl 2-(2-(benzyloxy)-5-nitrobenzamido)-4-phenylbenzoate (0.14 g) in methanol (1.4 mL) and acetic acid (1.4 mL), followed by heating to reflux for 1 hour. The reaction mixture was cooled to room temperature, and iron powder (14 mg) was added thereto, followed by heating to reflux for 30 minutes. The reaction mixture was cooled to room temperature, and a saturated aqueous solution of sodium bicarbonate and ethyl acetate were added thereto. The insoluble substance was removed by filtration. 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. The obtained residue was purified by silica gel column chromatography [Kanto Chemical Co., Inc., silica gel 60 (spherical), eluent: 90-50% hexane/ethyl acetate] to obtain 0.065 g of tert-butyl 2-(5-amino-2-(benzyloxy)benzamido)-4-phenylbenzoate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492582B2
Source datasetuspto-grants-2013_07
ORD IDord-185dd8b1c00149b9871b625514f9136e
Source noteuspto-grants-2013_07