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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132920생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/132920

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 0.96 g (5.0 mmol) of 1,2-dichloro-3-nitrobenzene and 0.93 g (5.0 mmol, 1 eq) of 1-tert-butyloxycarbonylpiperazine in acetonitrile (5 mL) was added 1.38 g (10 mmol, 2 eq) of K2CO3. The mixture was heated to reflux for 48 h. The solvent was removed under reduced pressure. The crude product was partitioned between EtOAc (100 mL) and 20 mL of H2O. The organic layer was washed with H2O (2×20 mL), dried over Na2SO4 and concentrated. Column chromatography (silica, 10-20% EtOAc/hexanes) provided 1.2 g (70%) of 4-(2-chloro-6-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester. TLC (silica, 20% EtOAc/hexanes): Rf=0.45. 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), 3.56-3.38 (m, 4H), 3.10-3.00 (m, 4H), 1.48 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388011B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-227bb913a3ec4273865c894e307e46fd
출처 메모uspto-grants-2008_06