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HRID 394492作成日:2026年10月24日

Hydrogen Bromide → 1-(2-Bromophenyl)-4-methylpiperazine

https://huagongshe.com/ja/reaction/394492

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Sodium HydroxideHCID 14798—
反応物2-(4-Methylpiperazin-1-yl)anilineHCID 286547—
反応物Sodium NitriteHCID 23668193—
触媒Copper bromide (CuBr2)HCID 24611—
溶媒WaterHCID 962—
生成物1-(2-Bromophenyl)-4-methylpiperazineHCID 12069432—

反応条件

温度22.5 °C

反応手順

A solution of 2-(4-methylpiperazin-1-yl)-aniline (23.77 grams, 0.124 mol) in 80 mL of 48% hydrobromic acid was cooled to 20° C. and treated with a solution of sodium nitrite (8.6 grams, 0.124 mol) in 35 mL of water while maintaining a temperature of 20-25° C. To this was added a solution of copper (II) bromide (3.5 grams, 0.024 mol) in 12 mL of 48% HBr. The mixture was heated to 85° C. for approximately 30 minutes, poured over crushed ice in a large beaker and neutralized with dilute aqueous sodium hydroxide. The crude product was extracted into diethyl ether and concentrated in vacuo to a black oil which was chromatographed on silica gel using triethylamine.methanol.methylene chloride (0.5:10:90) as the eluent. The product, 1-bromo-2-(4-methylpiperazin-1-yl)benzene, was obtained as a brown oil 20 grams Mass spectrum: 254 (M+), 256 1H-NMR (CDCl3, 300 MHz) δ 7.55 (1H, d), 7.30 (1H, t), 7.05 (1H, d), 6.9 (1H, t), 3.05 (4H, br s), 2.55 (4H, t), 2.35 (3H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06602874B2
出典データセットuspto-grants-2003_08
ORD IDord-66e6390c3d0f4e118c85e512c019fae9
出典メモuspto-grants-2003_08