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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21190Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/21190

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktPotassium IodideHCID 4875—
EduktNitric acid, 1,1-dimethylethyl esterHCID 164756—
Edukt7-Amino-2,3-dihydro-1H-isoindol-1-oneHCID 16228923—
Edukt7-Amino-4-methylisoindolin-1-oneHCID 53438682—
Edukt7-Iodo-4-methylisoindolinoneHCID 68489093—
KatalysatorCopper iodideHCID 83717—
LösungsmittelAcetonitrileHCID 6342—
Produkt7-Iodo-2,3-dihydro-1H-isoindol-1-oneHCID 4691188950%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745641B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-67c101f9644c4906b0a4a7cbf1725fa0
Quellennotizuspto-grants-2010_06