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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49810생성일: 2026년 10월 25일

Water → tert-Butyl 4-(3-aminophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/49810

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-Fluoro-3-nitrobenzeneHCID 9823—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물tert-Butyl 4-(3-aminophenyl)piperazine-1-carboxylateHCID 22330182—

반응 조건

온도120 °C

반응 단계

A mixture of tert-butyl 1-piperazinecarboxylate (4 g, 21.5 mmol) and 3-fluoronitrobenzene (2.3 ml, 21.5 mmol) in anhydrous NMP (5 ml) was heated to 120° C. for 3 days. After cooling water (25 ml) was added and the mixture was extracted with ethyl acetate (2×10 ml). The organic extract was dried over sodium sulfate and the solvent was removed under reduced pressure. The residue was purified by column-chromatography using successively petroleum ether and a mixture of ethyl acetate and petroleum ether (1:1 v/v) as the eluents. Yield of t-butyl 4-(3-nitrophenyl)-1-piperazinecarboxylate: 1.34 g (20%). This intermediate was quantitatively hydrogenated to 2g in ethanol at ambient pressure using Pd (5% on activated carbon) as the catalyst.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710044B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8c4a0f1e6ca24e1b99b4b254177998fe
출처 메모uspto-grants-2004_03