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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451473Generated: October 31, 2026

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

https://huagongshe.com/reaction/1451473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantTetrahydrofuranHCID 8028—
Reactant3-(2,5-Difluorobenzoyl)isonicotinic acidHCID 10015612—
Reactant4-(2,5-Difluorobenzoyl)nicotinic acidHCID 10467908—
SolventFuming sulfuric acidHCID 24681—
Product6,9-Difluorobenzo[g]isoquinoline-5,10-dioneHCID 10105904—

Reaction Steps

A solution of the mixture of 4-(2,5-difluorobenzoyl)nicotinic acid and 3-(2,5-difluorobenzoyl)isonicotinic acid of Preparative Example 2 (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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604246
Source datasetuspto-grants-1997_02
ORD IDord-2c709e8f6350484e8e69cbbf6da65443
Source noteuspto-grants-1997_02