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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57414생성일: 2026년 10월 24일

Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)- → 1-(4-chlorophenyl)-2-methyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/ko/reaction/57414

반응식

참여 물질

역할이름HCID투입량
반응물Bicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
반응물1-(4-chlorophenyl)-4-(1,3-dioxolan-2-yl)-2-methyl-1H-imidazoleHCID 90416014—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-(4-chlorophenyl)-2-methyl-1H-imidazole-4-carbaldehydeHCID 9041504269%

반응 단계

A solution of 1-(4-chlorophenyl)-4-(1,3-dioxolan-2-yl)-2-methyl-1H-imidazole (1.05 g, 3.97 mmol) and camphorsulfonic acid (92 mg, 0.40 mmol, 0.1 equiv) in THF (26.5 mL) and water (13.3 mL) was heated at 60° C. for 1 hour. The reaction was then cooled to room temperature and quenched with saturated aqueous sodium bicarbonate (100 mL). The mixture was extracted with ethyl acetate (100 mL) and the organic layer was washed with saturated aqueous sodium chloride (50 mL), dried (Na2SO4), filtered, and concentrated in vacuo. Silica gel column chromatography (EtOAc with 7% methanol) provided 1-(4-chlorophenyl)-2-methyl-1H-imidazole-4-carbaldehyde (0.600 g, tan solid) in 69% yield. 1H NMR (400 MHz, CDCl3) δ 9.89 (s, 1H), 7.67 (s, 1H), 7.53 (d, J=8.7 Hz, 2H), 7.27 (d, J=8.7 Hz, 2H), 2.40 (s, 3H). MS m/z 221.0 (M+H)+; Rt-0.47 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434719B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-f645c324388b4dbbbf9bf608ac3e8c3a
출처 메모uspto-grants-2016_09