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HRID 234807作成日:2026年10月26日

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

https://huagongshe.com/reaction/234807

反応式

関与物質

役割名称HCID仕込み量
反応物MethaneHCID 297—
反応物TetrahydrofuranHCID 8028—
反応物3-(2,5-Difluorobenzoyl)isonicotinic acidHCID 10015612—
反応物4-(2,5-Difluorobenzoyl)nicotinic acidHCID 10467908—
溶媒Fuming sulfuric acidHCID 24681—
生成物6,9-Difluorobenzo[g]isoquinoline-5,10-dioneHCID 10105904—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596097
出典データセットuspto-grants-1997_01
ORD IDord-b451e80a515e4e49ae6f78c9d85e0831
出典メモuspto-grants-1997_01