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HRID 652009Erstellt: 24. Oktober 2026

Potassium Iodide → 2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3(2H)-dione

https://huagongshe.com/de/reaction/652009

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
EduktPotassium CarbonateHCID 11430—
EduktNaphthalimideHCID 66491—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3(2H)-dioneHCID 20199012—

Reaktionsschritte

Eight-tenths mole (157.6 g.) of 1,8-naphthalimide, 260 g. (1.15 m.) of 4-chloro-3-nitrobenzotrifluoride, 64 g. (0.46 m.) of anhydrous potassium carbonate, about 4 g. (0.024 m.) of potassium iodide, and 2400 ml. of dry N,N-dimethylformamide were allowed to reflux under a nitrogen atmosphere for about 8 hours. The reaction mixture was allowed to cool to room temperature and the reaction vessel was then chilled in an ice-bath. The resulting precipitate was filtered, washed with water, and dried in vacuo to yield crude 2-[2-nitro-4-(trifluoromethyl)phenyl]-1H-benz[de]isoquinoline-1,3-(2H)-dione.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04670442
Quelldatensatzuspto-grants-1987_06
ORD IDord-82899705897a4bfa9bf9250d94b48d87
Quellennotizuspto-grants-1987_06