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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132912생성일: 2026년 10월 25일

Potassium Carbonate → 1-Boc-4-(2-chloro-6-nitrophenyl)piperazine

https://huagongshe.com/reaction/132912

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,3-DichloronitrobenzeneHCID 18555—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
용매AcetonitrileHCID 6342—
생성물1-Boc-4-(2-chloro-6-nitrophenyl)piperazineHCID 5876770470.2%

반응 단계

To a stirred solution of 1,2-dichloro-3-nitrobenzene (0.96 g, 5.0 mmol) and piperazine-1-carboxylic acid tert-butyl ester (0.93 g, 5.0 mmol) in acetonitrile (5 mL) was added of K2CO3 (1.38 g, 10 mmol). The mixture was heated at reflux for 48 h. The solvent was removed under reduced pressure. The crude material was partitoned between EtOAc (100 mL) and H2O (20 mL). The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (1.2 g, 70%). TLC (silica, 20% EtOAc/hexanes): Rf=0.45. MS (electrospray): exact mass calculated for C15H20CIN3O4, 341.1; m/z found, 364.1 [M+Na]30 . 1H NMR (400 MHz, CDCl3) 7.56 (dd, J=8.2, 1.4 Hz, 1H), 7.50 (dd, J=8.2, 1.4 Hz, 1H), 7.13 (t, J=8.2 Hz, 1H), 3.38-3.56 (m, 4H), 3.06 (m, 4H), 1.48 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388011B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-684344737d874f748b52592cd98fb8a5
출처 메모uspto-grants-2008_06