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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51298생성일: 2026년 10월 24일

Phenethyl bromide → 1-Phenethyl-1H-imidazole-4-carbaldehyde

https://huagongshe.com/ko/reaction/51298

반응식

참여 물질

역할이름HCID투입량
반응물Phenethyl bromideHCID 7666—
반응물Sodium hydrideHCID 24758—
반응물1H-Imidazole-4-carbaldehydeHCID 76428—
용매TetrahydrofuranHCID 8028—
생성물1-Phenethyl-1H-imidazole-4-carbaldehydeHCID 22289872—

반응 단계

Imidazole-4-carboxaldehyde (6.73 g, 70 mmol) was added portionwise to a suspension of sodium hydride (1.68 g, 60% dispersion in mineral oil, 70 mmol) in tetrahydrofuran (280 ml), and the mixture was then stirred at room temperature for 30 minutes. (2-Bromoethyl)benzene (9.56 ml, 70 mmol) was added, and the mixture was stirred at room temperature for 72 hours. The mixture was evaporated under reduced pressure and the residue was partitioned between water (300 ml) and dichloromethane (500 ml), and the layers were separated. The organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was pre-adsorbed onto silica gel, and purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (50:50 to 100:0) to afford the title compound, 1.44 g. 1H-NMR (CDCl3, 400 MHz) δ: 3.16 (t, 2H), 4.23 (t, 2H), 7.02 (d, 2H), 7.28 (m, 3H), 7.36 (s, 1H), 7.50 (s, 1H), 9.83 (s, 1H). LRMS: m/z (ES+) 223 [MNa+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713496B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-31441750fe72498fa9d8520b043eb1a1
출처 메모uspto-grants-2004_03