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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 409672생성일: 2026년 10월 24일

1-Bromo-4-nitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/ko/reaction/409672

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-4-nitrobenzeneHCID 11466—
반응물1-BenzylpiperazineHCID 75994—
용매Water methylene chlorideHCID 21908982—
생성물1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—

반응 조건

온도80 °C

반응 단계

A mixture of 1-bromo-4-nitrobenzene (5 g, 24.8 mmol) and 1-benzylpiperazine (8.6 ml, 49.5 mmol, 2 equiv) is heated to 80° C. for 17 h. The reaction mixture is allowed to cool to RT, and is diluted with DCM/H2O. The layers are separated and the aqueous phase is extracted with DCM. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the residue by silica gel column chromatography (Hex/EtOAc, 1:1) affords the title compound as a yellow solid: ESI-MS: 298.3 [MH]+; tR=3.25 min (purity: 100%, system 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759517B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-58bd338a40824640897be00271babb1d
출처 메모uspto-grants-2014_06