Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21093Generated: October 27, 2026

Iodine → 7-Iodo-4-(furan-2-yl)isoindolinone

https://huagongshe.com/reaction/21093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium IodideHCID 4875—
ReactantTert-Butyl nitriteHCID 10906—
Reactant7-Amino-4-(furan-2-yl)isoindolinoneHCID 68492739—
CatalystCopper iodideHCID 83717—
SolventAcetonitrileHCID 6342—
Product7-Iodo-4-(furan-2-yl)isoindolinoneHCID 6848748758%

Reaction Steps

In a similar manner to Step 4 of Example 140, 7-amino-4-(furan-2-yl)isoindolinone (43.0 mg, 0.201 mmol) was dissolved in acetonitrile (4.3 mL), and the solution was treated with potassium iodide (40.0 mg, 0.241 mmol), copper iodide (46.0 mg, 0.241 mmol), iodine (61.0 mg, 0.241 mmol) and tert-butyl nitrite (0.072 mL, 0.60 mmol), followed by purification by preparative thin-layer chromatography (chloroform/acetonitrile=6/1) to obtain 7-iodo-4-(furan-2-yl)isoindolinone (37.8 mg, yield 58%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745641B2
Source datasetuspto-grants-2010_06
ORD IDord-af72a1588c2f4fcfb3ce709ff335d054
Source noteuspto-grants-2010_06