Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351225Generated: November 2, 2026

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

https://huagongshe.com/reaction/2351225

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 ethanol, 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 numberUS04871842
Source datasetuspto-grants-1989_10
ORD IDord-b44662a576d242629dc4e7ee963a3805
Source noteuspto-grants-1989_10