돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 650924생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/650924

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen BromideHCID 260—
반응물Sodium HydroxideHCID 14798—
반응물2-(4-Methylpiperazin-1-yl)anilineHCID 286547—
반응물Sodium NitriteHCID 23668193—
촉매Copper bromide (CuBr2)HCID 24611—
용매WaterHCID 962—
생성물1-(2-Bromophenyl)-4-methylpiperazineHCID 12069432—

반응 조건

온도22.5 °C

반응 단계

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) δ7.55 (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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06277852B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-72b8e0e9ba1f4bc2b2f3968847ee08fd
출처 메모uspto-grants-2001_08