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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 858425생성일: 2026년 10월 26일

1,3-Dichloro-2-nitrobenzene → 2-[4-(3-Chloro-2-nitroanilino)phenyl]ethanol

https://huagongshe.com/reaction/858425

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Dichloro-2-nitrobenzeneHCID 11759—
반응물4-Aminophenethyl alcoholHCID 66904—
반응물Sodium AcetateHCID 517045—
용매WaterHCID 962—
생성물2-[4-(3-Chloro-2-nitroanilino)phenyl]ethanolHCID 2187584972%

반응 조건

온도160 °C

반응 단계

A mixture of 2,6-dichloronitrobenzene (Norman, M. H.; Chen, N.; et al. PCT Int. Appl., WO 9940091 (1999)., Spada, A. P.; Fink, C. A.; Myers, M. R. PCT Int. Appl., WO 9205177 (1992)., 6.3 g, 32.8 mmol), 4-aminophenylethyl alcohol (4.9 g, 36 mmol) and sodium acetate (3.2 g, 39.3 mmol) was placed in a sealed tube and heated at 160° C. for 3 h. After cooling, the mixture was poured into water (100 mL) and extracted with ethyl acetate (300 mL). The organic layer was washed with 2N aqueous NaOH (100 mL) and brine (100 mL), then dried (Na2SO4), and concentrated. Purification by flash column chromatography on silica gel eluting with hexane/ethyl acetate (1:1) to afford 4.57 g (72%) of the title compound as a red oil: 1H-NMR (CDCl3) δ 7.09–7.28 (6H, m), 6.91 (1H, dd, J=2.0, 7.1 Hz), 3.87 (2H, t, J=6.6 Hz), 2.86 (2H, t J=6.6 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07148234B2
출처 데이터셋uspto-grants-2006_12
ORD IDord-28c23d5b2037450aa8d02bb33d48c492
출처 메모uspto-grants-2006_12