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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57412생성일: 2026년 10월 23일

Ethylene Glycol → 1-(4-chlorophenyl)-4-(1,3-dioxolan-2-yl)-1H-imidazole

https://huagongshe.com/ko/reaction/57412

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
반응물1-(4-chlorophenyl)-1H-imidazole-4-carbaldehydeHCID 83883034—
용매TolueneHCID 1140—
생성물1-(4-chlorophenyl)-4-(1,3-dioxolan-2-yl)-1H-imidazoleHCID 9041646141.2%

반응 단계

A solution of ethane-1,2-diol (0.081 mL, 1.45 mmol, 1.5 equiv), 1-(4-chlorophenyl)-1H-imidazole-4-carbaldehyde (200 mg, 0.968 mmol), and camphorsulfonic acid (45 mg, 0.19 mmol, 0.2 equiv) in toluene (10 mL) was heated at reflux with a Dean-Stark apparatus for 1 hour. The reaction was cooled to room temperature and quenched with saturated aqueous sodium bicarbonate (30 mL). The mixture was extracted with ethyl acetate (30 mL) and the organic layer was dried (Na2SO4), filtered, and concentrated in vacuo. Silica gel column chromatography (EtOAc with 7% methanol) provided 1-(4-chlorophenyl)-4-(1,3-dioxolan-2-yl)-1H-imidazole (0.100 g, tan solid) in 41% yield. 1H NMR (400 MHz, CDCl3) δ 7.80 (s, 1H), 7.46 (d, J=8.4 Hz, 2H), 7.36 (s, 1H), 7.33 (d, J=8.4 Hz, 2H), 5.96 (s, 1H), 4.20 (m, 2H), 4.05 (m, 2H). MS m/z 251.0 (M+H)+; Rt-0.53 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-cbb27b2855364653acd1451f26169498
출처 메모uspto-grants-2016_09