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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645063Generated: November 1, 2026

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

https://huagongshe.com/reaction/1645063

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 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 NM (DMSO-d6) δ 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 numberUS08124630B2
Source datasetuspto-grants-2012_02
ORD IDord-f4c568df9b954f8bb5904869b0ebe453
Source noteuspto-grants-2012_02