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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031814Generated: November 1, 2026

4-(2-Nitrophenyl)-2-phthalimidobutyric acid → 4-(2-Aminophenyl)-2-phthalimidobutyric acid

https://huagongshe.com/reaction/1031814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-Nitrophenyl)-2-phthalimidobutyric acidHCID 14407251—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product4-(2-Aminophenyl)-2-phthalimidobutyric acidHCID 1401068184.9%

Reaction Steps

In 300 ml of methanol, 13 g of 4-(2-nitrophenyl)-2-phthalimidobutyric acid is catalytically reduced at ambient temperature and under atmospheric pressure with use of 3 g of 5% palladium-carbon as a catalyst. After the calculated amount of hydrogen is absorbed, the insoluble material is separated by filtration, and washed four times with 300 ml of acetone. The acetone washings and the methanol portion are combined and concentrated under reduced pressure. The residue is admixed with 50 ml of ethaniol, and the crystals which separate out are collected by filtration to give 10.1 g of 4-(2-aminophenyl)-2-phthalimidobutyric acid as yellow prisms, m.p. 198°-203° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954625
Source datasetuspto-grants-1990_09
ORD IDord-a57a2a8f53134ba7a1e9bf725a729056
Source noteuspto-grants-1990_09