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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21190Generated: October 27, 2026

Iodine → 7-Iodo-2,3-dihydro-1H-isoindol-1-one

https://huagongshe.com/reaction/21190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
ReactantNitric acid, 1,1-dimethylethyl esterHCID 164756—
Reactant7-Amino-2,3-dihydro-1H-isoindol-1-oneHCID 16228923—
Reactant7-Amino-4-methylisoindolin-1-oneHCID 53438682—
Reactant7-Iodo-4-methylisoindolinoneHCID 68489093—
CatalystCopper iodideHCID 83717—
SolventAcetonitrileHCID 6342—
Product7-Iodo-2,3-dihydro-1H-isoindol-1-oneHCID 4691188950%

Reaction Steps

In a similar manner to Step 4 of Example 140, a mixture of 7-amino-4-methylisoindolinone and 7-aminoisoindolinone (10/1, 57.4 mg, 0.357 mmol) was dissolved in acetonitrile (4.6 mL), and the solution was treated with potassium iodide (78 mg, 0.47 mmol), copper iodide (90 mg, 0.47 mmol), iodine (120 mg, 0.471 mmol) and tert-butyl nitrate (0.128 mL, 1.07 mmol), followed by purification by preparative thin-layer chromatography (chloroform/acetonitrile=5/1) to obtain a mixture of 7-iodo-4-methylisoindolinone and 7-iodoisoindolinone (44.8 mg, ratio 10/1, yield 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-67c101f9644c4906b0a4a7cbf1725fa0
Source noteuspto-grants-2010_06