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HRID 1060002作成日:2026年10月26日

Sodium Carbonate → 4-(4-Methoxypyridin-2-yl)-2-nitrotoluene

https://huagongshe.com/reaction/1060002

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-Methyl-3-nitrobenzeneboronic acidHCID 2773515—
反応物2-Bromo-4-methoxypyridineHCID 4738484—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Methoxypyridin-2-yl)-2-nitrotolueneHCID 1863100395.1%

反応条件

温度80 °C

反応手順

To a suspension of 2-bromo-4-methoxypyridine (2.5 g), 4-methyl-3-nitrophenylboronic acid (3.37 g) and tetrakis(triphenylphosphine)-palladium (768 mg) in 1,2-dimethoxyethane (100 ml) was added 2M aqueous solution of sodium carbonate (18.6 ml). The mixture was stirred at 80° C. for 7 hours under a nitrogen atmosphere, then cooled to room temperature and diluted with ethyl acetate. The organic layer was separated, washed with water and brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure. Methanol was added to the residue. The precipitate was collected by filtration and dried under reduced pressure to give 4-(4-methoxypyridin-2-yl)-2-nitrotoluene (3.09 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06521643B1
出典データセットuspto-grants-2003_02
ORD IDord-095fc507c68f4166bbaf3abdc528761d
出典メモuspto-grants-2003_02