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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475716생성일: 2026년 10월 26일

Water → 1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole

https://huagongshe.com/reaction/475716

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Potassium HydroxideHCID 14797—
반응물2-Chloro-5-nitroanisoleHCID 70519—
반응물HCID 178418800HCID 178418800—
용매Dimethyl SulfoxideHCID 679—
생성물1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 4548018020.5%

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온도110 °C

반응 단계

A mixture of 4-methyl-1H-imidazole (18.0 g, 53.5 mmol), 1-chloro-2-methoxy-4-nitrobenzene (10.0 g, 53.5 mmol), and potassium hydroxide (4.5 g, 80.3 mmol) in DMSO (50 mL) was heated at 110° C. for 24 h. The reaction mixture was allowed to cool to rt and was poured into 1000 mL of water. The aqueous mixture was extracted with dichloromethane (3×250 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The crude reaction mixture was purified using silica gel chromatography (330 g silica cartridge, 0-2% MeOH/chloroform, linear gradient over 72 min, flow 25 mL/min) to afford 1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole (2.56 g, 20% yield) as a yellow/orange solid. LC-MS (M+H)+=234.1. 1H NMR (500 MHz, CDCl3) δ ppm 7.97-8.00 (m, 1H) 7.93-7.97 (m, 2H) 7.45 (d, J=8.85 Hz, 1H) 7.02 (s, 1H) 4.02 (s, 3H) 2.35 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637525B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-ca0ee2577273421dbefc3b77a3674f24
출처 메모uspto-grants-2014_01