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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859155Generated: October 26, 2026

1H-Isoindole-1,3(2H)-dione, 2-(2-nitrophenyl)- → 2-(2-Aminophenyl)isoindole-1,3-dione

https://huagongshe.com/reaction/859155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-nitrophenyl)-HCID 101313—
SolventBenzeneHCID 241—
Product2-(2-Aminophenyl)isoindole-1,3-dioneHCID 67367640%

Reaction Steps

To a suspension of the 2-(2-nitrophenyl)isoindole-1,3-dione (1.0 g, 3.50 mmol) in benzene, pre-sparged with nitrogen gas, was added 10% palladium on activated carbon (1.0 g). The reaction mixture was placed under an atmosphere of hydrogen gas and was vigorously stirred. After 45 minutes, the reaction mixture was filtered over celite and the filter pad was washed with benzene. Concentration in vacuo gave 236 mg (40%) of 2-(2-aminophenyl)-isoindole-1,3-dione as a yellow solid: 1H NMR (300 MHz, DMSO-d6) δ 8.85 (m, 4H), 7.10 (m, 1H), 6.98 (m, 1H), 6.75 (m, 1H), 6.55 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151112B1
Source datasetuspto-grants-2006_12
ORD IDord-2ea360f61f494f539fd7449e40c062fa
Source noteuspto-grants-2006_12