Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898942Generated: October 31, 2026

5-(4-Nitrophenoxy)-1H-isoindole-1,3(2H)-dione → 5-(4-Aminophenoxy)isoindoline-1,3-dione

https://huagongshe.com/reaction/898942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Nitrophenoxy)-1H-isoindole-1,3(2H)-dioneHCID 867501—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-(4-Aminophenoxy)isoindoline-1,3-dioneHCID 88262775%

Reaction Steps

A solution of 5-(4-nitrophenoxy)isoindoline-1,3-dione (0.6 g, 2.11 mmol) in conc. AcOH (12 mL) and water (0.1 mL) was stirred under a stream of argon while iron powder (0.59 g, 55.9 mmol) was added slowly. This mixture stirred at room temp. for 72 h, then was diluted with water (25 mL) and extracted with EtOAc (3×50 mL). The combined organic layers were dried (MgSO4) and concentrated under reduced pressure to give 5-(4-aminophenoxy)isoindoline-1,3-dione as a brownish solid (0.4 g, 75%): TLC (50% EtOAc/50% hexane) Rf 0.27; 1H NMR (DMSO-d6) □5.14 (br s, 2H), 6.62 (d, J=8.7 Hz, 2H), 6.84 (d, J=8.7 Hz, 2H), 7.03 (d, J=2.1 Hz, 1H), 7.23 (dd, 1H), 7.75 (d, J=8.4 Hz, 1H), 11.02 (s, 1H); HPLC ES-MS m/z 255 ((M+H)+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351834B1
Source datasetuspto-grants-2008_04
ORD IDord-062363f408f94e71a6b21bdbfaa8232b
Source noteuspto-grants-2008_04