戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2387509作成日:2026年10月25日

Potassium Carbonate → (E)-2-Methoxy-4-styrylpyridine

https://huagongshe.com/reaction/2387509

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Styrylboronic acidHCID 5702628—
反応物4-Bromo-2-methoxypyridineHCID 14062309—
溶媒Dimethyl SulfoxideHCID 679—
生成物(E)-2-Methoxy-4-styrylpyridineHCID 5795030693%

反応条件

温度90 °C

反応手順

4-Bromo-2-methoxypyridine (1.85 g, 9.84 mmol), (E)-phenylvinylboronic acid (4.3 g, 30 mmol), K2CO3 (4.0 g, 30 mmol) and [1,1′-Bis-(diphosphenylphosphino)ferrocene]dichloropalladium(II) (PdCl2dppf) (400 mg, 0.5 mmol) were stirred in DMSO (15 mL) under vacuum for 30 min. The flask was flushed with nitrogen and the mixture was heated at 90° C. for 30 min. Upon cooling, the mixture was diluted with methylene chloride and washed with 5% lithium chloride solution (5×), dried, concentrated, and the residue was purified by column chromatography (silica gel, hexanes/ethyl acetate, 97:3 to 75:25) to provide the title compound (1.93 g, 93%) as an orange oil: 1H NMR (300 MHz, CDCl3) δ 8.12 (d, J=5.2 Hz, 1H), 7.51 (m, 2H), 7.40-7.22 (m, 4H), 7.02-6.94 (m, 2H), 6.78 (s, 1H), 3.95 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08268868B2
出典データセットuspto-grants-2012_09
ORD IDord-447a5dfefe9e400dbca9900739780589
出典メモuspto-grants-2012_09