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HRID 571作成日:2026年10月23日

Aniline → N-phenylpyridin-4-amine

https://huagongshe.com/ja/reaction/571

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物4-BromopyridineHCID 14268—
試薬Sodium t-butoxideHCID 23676156—
触媒1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
触媒Palladium (II) acetateHCID 4144353—
溶媒TolueneHCID 1140—
生成物N-phenylpyridin-4-amineHCID 8994524.88%

反応条件

温度100 °C

反応手順

ANILINE (3.94 mL, 43.29 mmol) was added to 4-bromopyridine (5.7 g, 36.08 mmol), PALLADIUM(II) ACETATE (0.162 g, 0.72 mmol), XANTPHOS (1.252 g, 2.16 mmol) and SODIUM TERT-BUTOXIDE (4.85 g, 50.51 mmol) in toluene (280 mL) under nitrogen. The resulting mixture was stirred at 100 °C for 4 hours. The reaction mixture was evaporated to dryness and redissolved in EtOAc (200 mL), and washed sequentially with water (2 x 100 mL) and saturated brine (100 mL). The organic layer was dried over MgSO4, filtered and preadsorbed onto silica. The crude product was purified by flash silica chromatography, elution gradient 0 to 100% EtOAc in heptane. Pure fractions were evaporated to dryness to afford N-phenylpyridin-4-amine (1.528 g, 24.88 %) as a pink solid.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-72db1f71b9ee4c528872b1ba0810230a
出典メモ750 AstraZeneca ELN dataset