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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768285Generated: November 1, 2026

5-Hydroxyisoindoline-1,3-dione → 5-Hydroxy-2,3-dihydro-1H-isoindol-1-one

https://huagongshe.com/reaction/1768285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Hydroxyisoindoline-1,3-dioneHCID 10558950—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product5-Hydroxy-2,3-dihydro-1H-isoindol-1-oneHCID 2259420720.9%

Reaction Steps

To a solution of 5-hydroxyphthalimide (19.8 g, 121 mmol) in AcOH (500 mL) was slowly added zinc dust (47.6 g, 729 mmol) in portions, then the mixture was heated at the reflux temp. for 40 min., filtered hot, and concentrated under reduced pressure. The reaction was repeated on the same scale and the combined oily residue was purified by column chromatography (1.1 Kg SiO2; gradient from 60% EtOAc/40% hexane to 25% MeOH/75% EtOAc) to give 5-hydroxyisoindolin-1-one (3.77 g): TLC (100% EtOAc) Rf 0.17; HPLC ES-MS m/z 150 ((M+H)+). Step 2. Synthesis of 4-(1-isoindolinon-5-yloxy)-1-nitrobenzene

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235576B1
Source datasetuspto-grants-2007_06
ORD IDord-e9961ab258f4468e9354010ed60808fb
Source noteuspto-grants-2007_06