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HRID 234807Erstellt: 24. Oktober 2026

Methane → 6,9-Difluorobenzo[g]isoquinoline-5,10-dione

https://huagongshe.com/de/reaction/234807

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktTetrahydrofuranHCID 8028—
Edukt3-(2,5-Difluorobenzoyl)isonicotinic acidHCID 10015612—
Edukt4-(2,5-Difluorobenzoyl)nicotinic acidHCID 10467908—
LösungsmittelFuming sulfuric acidHCID 24681—
Produkt6,9-Difluorobenzo[g]isoquinoline-5,10-dioneHCID 10105904—

Reaktionsschritte

A solution of the mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)isonicotinic acid of Preparative Example 3 (61.07 g) in 20% oleum (100 mL) is heated at 140° C. while 20% oleum is added in four portions (13.2 mL each) at 20 min-intervals. After the fourth addition the mixture is heated for 20 min, then it is cooled to room temperature and quenched with a mixture of ice (1,500 g), water (1,500 mL) and 35% NaOH (350 mL). The mixture is extracted four times with methylene chloride (1×1,000 mL followed by 3×500 mL). The combined organic solutions are washed with water (2×1,000 mL), dried (Na2SO4) and the solvent removed by roto-evaporation. The dark-red solid obtained (56.0 g) is dissolved in boiling THF (840 mL) and decolorizing charcoal (8.40 g) is added. After 30 min the mixture is filtered while hot and the filtrate concentrated to 200 mL. The precipitate obtained is collected by suction filtration to give 6,9-difluorobenzo[g]isoquinoline-5,10-dione (43.00 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05596097
Quelldatensatzuspto-grants-1997_01
ORD IDord-b451e80a515e4e49ae6f78c9d85e0831
Quellennotizuspto-grants-1997_01