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HRID 892739作成日:2026年10月25日

Hydrazine hydrate (1:1) → 4-(Quinolin-2-ylmethoxy)aniline

https://huagongshe.com/reaction/892739

反応式

関与物質

役割名称HCID仕込み量
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 added and the mixture was warmed to 35° C. 63.1 g (1.26 mol) of hydrazine hydrate 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 solution was then washed with water and conc. hydrochloric acid was added to the organic phase. The precipitate which deposited was filtered off, washed with 2N hydrochloric acid and dissolved in water, and the solution was 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US05120744
出典データセットuspto-grants-1992_06
ORD IDord-2e4cd6db82ee48a7960663130937bec4
出典メモuspto-grants-1992_06