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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78314Generated: October 29, 2026

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

https://huagongshe.com/reaction/78314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantSodium hydrideHCID 24758—
Reactant5-Hydroxy-2,3-dihydro-1H-isoindol-1-oneHCID 22594207—
SolventDimethylformamideHCID 6228—
Product1h-Isoindol-1-one,2,3-dihydro-5-(4-nitrophenoxy)-HCID 2313724789%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a slurry of NaH (0.39 g, 16.1 mmol) in DMF at 0° C. was added 5-hydroxyisoindolin-1-one (2.0 g, 13.4 mmol) in portions. The resulting slurry was allowed to warm to room temp. and was stirred for 45 min., then 4-fluoro-1-nitrobenzene was added and then the mixture was heated at 70° C. for 3 h. The mixture was cooled to 0° C. and treated with water dropwise until a precipitate formed. The resulting solids were collected to give 4-(1-isoindolinon-5-yloxy)-1-nitrobenzene as a dark yellow solid (3.23 g, 89%): TLC (100% EtOAc) Rf 0.35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841330B2
Source datasetuspto-grants-2014_09
ORD IDord-220a169bb78443589d9fd5e713f289df
Source noteuspto-grants-2014_09