戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 525984作成日:2026年10月27日

Phenyl-1-naphthylamine → N-(4-methoxyphenyl)-N-phenylnaphthalen-1-amine

https://huagongshe.com/reaction/525984

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl-1-naphthylamineHCID 7013—
反応物Potassium CarbonateHCID 11430—
反応物18-Crown-6HCID 28557—
反応物4-IodoanisoleHCID 69676—
触媒CopperHCID 23978—
溶媒DimethylformamideHCID 6228—
生成物N-(4-methoxyphenyl)-N-phenylnaphthalen-1-amineHCID 2297398135%

反応手順

A mixture of N-phenylnaphthalen-1-amine (5.0 g, 22.8 mmol), 4-iodoanisole (8.0 g, 34.2 mmol), copper powder (2.89 g, 45.6 mmol), K2CO3 (12.59 g, 91.2 mmol) and 18-crown-6 (0.607 g, 2.3 mmol) in DMF (200 mL) was degassed and heated to reflux for overnight under argon. After the salt and copper were filtered off, the solution was poured into water (300 mL), and extracted with DCM (2×300 mL). The organic phase was combined and washed with brine, dried over Na2SO4, loaded on silica gel, purified by flash column (5 to 20% DCM in hexanes). The desired fraction was collected, concentrated, and recrystallized in ethyl acetate/methanol to obtain a white solid (Compound 5) (2.59 g, in 35% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09343684B2
出典データセットuspto-grants-2016_05
ORD IDord-59e09aff113d4b98b0a32299a09ecac6
出典メモuspto-grants-2016_05