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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672836Generated: October 26, 2026

Iodine → 5-Iodoisoindoline-1,3-dione

https://huagongshe.com/reaction/1672836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantIsoamyl NitriteHCID 8053—
ReactantCesium iodideHCID 24601—
ReactantHydrogen iodideHCID 24841—
Reactant4-AminophthalimideHCID 72915—
ReactantSodium BicarbonateHCID 516892—
CatalystCopper iodideHCID 83717—
SolventAcetonitrileHCID 6342—
Product5-Iodoisoindoline-1,3-dioneHCID 2125757647%

Reaction Steps

Commercially available 4-aminophthalimide (500 mg, 3.08 mmol) was dissolved in acetonitrile (15 mL). To the mixture were added cesium iodide (961 mg, 3.70 mmol), iodine (947 mg, 3.70 mmol), and copper iodide (712 mg, 3.70 mmol) at room temperature, and then an 11% aqueous hydrogen iodide solution (15 mL) and isoamyl nitrite (1.24 mL, 9.24 mmol) at 0° C. The mixture was stirred at room temperature for 6.5 hours, and then for 1.5 hours after adding isoamyl nitrite (4.96 mL, 37.0 mmol). Then, saturated sodium bicarbonate was added to the mixture, and after filtration through sellite, the organic layer was separated. The resulting organic layer was washed with a saturated aqueous sodium thiosulfate solution and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was triturated with chloroform, and the resulting solid was filtered off and dried to give 4-iodophthalimide (394 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998954B2
Source datasetuspto-grants-2011_08
ORD IDord-5bd6e29d696f4872a4bf8d75fc2e4a20
Source noteuspto-grants-2011_08