Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877279Generated: November 2, 2026

Tetrahydrofuran → Ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate

https://huagongshe.com/reaction/1877279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 3-[methyl(4-nitrobenzoyl)amino]propanoateHCID 61794881—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductEthyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoateHCID 46941342112%

Reaction Steps

A mixture of ethyl 3-[methyl(4-nitrobenzoyl)amino]propanoate (26.6 g) synthesized above, 5% palladium-carbon (8.9 g), tetrahydrofuran (150 mL) and ethanol (150 mL) was stirred at room temperature overnight under a hydrogen atmosphere. 5% palladium-carbon was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2, volume ratio) to give the title compound (26.6 g, 90%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-78538291b8c54fa1a647cedd5bfc58d1
Source noteuspto-grants-2012_11