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HRID 85199作成日:2026年10月23日

Benzene, 1-fluoro-2-methyl-4-nitro- → 3-Bromo-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one

https://huagongshe.com/ja/reaction/85199

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-fluoro-2-methyl-4-nitro-HCID 68001—
反応物3-Bromo-2-hydroxypyridineHCID 818549—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物3-Bromo-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-oneHCID 59410157—

反応条件

温度80 °C

反応手順

44.5 g (280 mmol) of 3-bromopyridin-2(1H)-one are dissolved in 750 ml of anhydrous dimethyl sulphoxide, and 33.4 g (298 mmol) of potassium tert-butoxide are added a little at a time at room temperature. The suspension is stirred at this temperature for 1 h, 38.5 g (280 mmol) of 1-fluoro-2-methyl-4-nitrobenzene are then added and the reaction solution is heated at 80° C. for 20 h. The solution is allowed to cool and carefully diluted with water. The resulting crystalline precipitate is filtered off, washed with a little water and dried under reduced pressure. This gives 62 g (80% of theory) of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846934B2
出典データセットuspto-grants-2014_09
ORD IDord-9e774df9c76447548e29e9f21de0266e
出典メモuspto-grants-2014_09