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HRID 1059920作成日:2026年10月27日

3-Nitrophenylboronic Acid → 3-(4-Methoxypyridin-2-yl)-nitrobenzene

https://huagongshe.com/reaction/1059920

反応式

関与物質

役割名称HCID仕込み量
反応物3-Nitrophenylboronic AcidHCID 1677—
反応物Sodium CarbonateHCID 10340—
反応物2-Bromo-4-methoxypyridineHCID 4738484—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒DichloromethaneHCID 6344—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3-(4-Methoxypyridin-2-yl)-nitrobenzeneHCID 1866758461.7%

反応条件

温度90 °C

反応手順

To a suspension of 2-bromo-4-methoxypyridine (483 mg), 3-nitrophenylboronic acid (643 mg) and tetrakis(triphenylphosphine)-palladium (148 mg) in 1,2-dimethoxyethane (10 ml) was added 2M aqueous solution of sodium carbonate (2.78 ml). The mixture was stirred at 90° C. for 6 hours under a nitrogen atmosphere, then cooled to room temperature and diluted with dichloromethane. The organic layer was separated, washed with water and brine and dried over sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by column chromatography (silica gel 40 g, 50-100% dichloromethane in n-hexane) to give 3-(4-methoxypyridin-2-yl)-nitrobenzene (365 mg).

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-717226425c9d4f4e9fbc40d41e0a04bb
出典メモuspto-grants-2003_02