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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78315Generated: October 30, 2026

1h-Isoindol-1-one,2,3-dihydro-5-(4-nitrophenoxy)- → 1h-Isoindol-1-one,5-(4-aminophenoxy)-2,3-dihydro-

https://huagongshe.com/reaction/78315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1h-Isoindol-1-one,2,3-dihydro-5-(4-nitrophenoxy)-HCID 23137247—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1h-Isoindol-1-one,5-(4-aminophenoxy)-2,3-dihydro-HCID 23137216—

Reaction Steps

A slurry of 4-(1-isoindolinon-5-yloxy)-1-nitrobenzene (2.12 g, 7.8 mmol) and 10% Pd/C (0.20 g) in EtOH (50 mL) was stirred under an H2 atmosphere (balloon) for 4 h, then filtered through a pad of Celite®. The filtrate was concentrated under reduced pressure to afford 4-(1-oxoisoindolin-5-yloxy)aniline as a dark yellow solid: TLC (100% EtOAc) Rf 0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-a07a612fb477410a8caa0005ccd6d758
Source noteuspto-grants-2014_09