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HRID 727806作成日:2026年10月27日

Water → 4-(Quinolin-2-ylmethoxy)aniline

https://huagongshe.com/reaction/727806

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物2-[(4-Nitrophenoxy)methyl]quinolineHCID 13770360—
触媒NickelHCID 935—
溶媒MeOH tetrahydrofuranHCID 21899815—
生成物4-(Quinolin-2-ylmethoxy)anilineHCID 2747569—

反応条件

温度35 °C

反応手順

117.8 g (0.42 mol) of 2-(4-nitrophenoxymethyl)quinoline were dissolved in 1 l of methanol/tetrahydrofuran (1:1). About 5 g of Raney nickel were then added and the mixture was warmed to 35° C. 63.1 g (1.26 mol) of hydrazine hydrate ×H2O were then added dropwise and the mixture was stirred overnight. The residue was filtered off, the solution was concentrated in vacuo and the residue was taken up with methylene chloride. The mixture was then washed with water and conc. hydrochloric acid was added to the organic phase. The precipitate deposited was filtered off, washed with 2 N hydrochloric acid, dissolved in water and rendered alkaline with 20% strength NaOH. The residue was dried in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05045547
出典データセットuspto-grants-1991_09
ORD IDord-ed44bba192c04457973ed487570d6496
出典メモuspto-grants-1991_09