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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1262071생성일: 2026년 10월 26일

Acetic Acid → 2-Chloro-4-(4-methylpiperazin-1-yl)aniline

https://huagongshe.com/reaction/1262071

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물1-(3-Chloro-4-nitrophenyl)-4-methylpiperazineHCID 23139607—
촉매IronHCID 23925—
용매TetrahydrofuranHCID 8028—
생성물2-Chloro-4-(4-methylpiperazin-1-yl)anilineHCID 5741609425%

반응 조건

온도35 °C

반응 단계

1-(3-Chloro-4-nitro-phenyl)-4-methyl-piperazine (2.016 g, 7.885 mmol) was combined with Tetrahydrofuran (30 mL). The resulting mixture was filtered. The filtrate was combined with Acetic acid (40 mL, 700 mmol), then at room temperature Iron (2932 mg, 52.50 mmol) was added neat and the mixture was warmed to 35° C. under a nitrogen atmosphere. After 16 h filtered mixture and concentrated resulting filtrate under reduced pressure. The concentrated residue was partitioned between CHCl3 (2×) and saturated aqueous NaHCO3. Combined organics, dried over Na2SO4, filtered, and concentrated under reduced pressure to yield 0.44 g (25%) of 2-Chloro-4-(4-methyl-piperazin-1-yl)-phenylamine as a yellow tinted oil, which crystallized on sitting. This material was used without further manipulation for the subsequent step. LC/MS (E/I+) 226.05 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08471005B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-f20b74768544417ca913d27e5a2d0121
출처 메모uspto-grants-2013_06