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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648730Generated: October 25, 2026

N-(4-Nitrobenzoyl)-beta-alanine → N-(4-Aminobenzoyl)-beta-alanine

https://huagongshe.com/reaction/1648730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Nitrobenzoyl)-beta-alanineHCID 591374—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(4-Aminobenzoyl)-beta-alanineHCID 719629—

Reaction Steps

A suspension of 15 g. finely powdered 4-nitrobenzoyl-β-alanine in 200 ml. ethanol was stirred in an atmosphere of hydrogen in the presence of 1 g. of palladium-charcoal (5%), while cooling gently. When the absorption of hydrogen had ceased, the reaction mixture was filtered and the filtrate concentrated to a small volume. Upon adding diethyl ether and cooling, 4-aminobenzoyl-β-alanine was obtained. The yield was 11.5 g.; m.p. 156°-158° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04412992
Source datasetuspto-grants-1983_11
ORD IDord-5d0d7d473fa1422ba7376a1e74cf250c
Source noteuspto-grants-1983_11