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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 409671생성일: 2026년 10월 24일

Ethanol → 4-(4-Benzylpiperazin-1-yl)aniline

https://huagongshe.com/ko/reaction/409671

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물WaterHCID 962—
반응물1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—
촉매IronHCID 23925—
용매Acetic AcidHCID 176—
생성물4-(4-Benzylpiperazin-1-yl)anilineHCID 737259—

반응 조건

온도80 °C

반응 단계

Iron powder (5.4 g, 97 mmol, 4 equiv) is added portionwise to an 80° C. mixture of 1-benzyl-4-(4-nitro-phenyl)-piperazine (7.2 g, 24.2 mmol), EtOH (150 mL), H2O (40 mL), and AcOH (20 mL). The reaction mixture is stirred for 1.75 h at 80° C., allowed to cool to RT, and concentrated. The residue is diluted with EtOAc and an aqueous saturated solution of Na2CO3. The layers are separated and the aqueous phase is extracted with EtOAc. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated to afford the title compound: ES-MS: 268.3 [MH]+; single peak at tR=1.30 min (system 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759517B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-9ac1155e7ef04fc7ab35e1595741496c
출처 메모uspto-grants-2014_06