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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 51297생성일: 2026년 10월 23일

(2-Bromoethyl)cyclohexane → 1-(2-Cyclohexylethyl)-1H-imidazole-4-carboxaldehyde

https://huagongshe.com/ko/reaction/51297

반응식

참여 물질

역할이름HCID투입량
반응물(2-Bromoethyl)cyclohexaneHCID 15440—
반응물Sodium hydrideHCID 24758—
반응물1H-Imidazole-4-carbaldehydeHCID 76428—
용매TetrahydrofuranHCID 8028—
생성물1-(2-Cyclohexylethyl)-1H-imidazole-4-carboxaldehydeHCID 22289845—

반응 단계

Imidazole-4-carboxaldehyde (4.8 g, 50 mmol) was added portionwise to a suspension of sodium hydride (2.20 g, 60% dispersion in mineral oil, 55 mmol) in tetrahydrofuran (150 ml), and the mixture was then stirred at room temperature for 1 hour. 2-Cyclohexylethyl bromide (8.6 ml, 55 mmol) was added, and the mixture was heated under reflux for 18 hours. The cooled mixture was evaporated under reduced pressure and the residue was partitioned between water (500 ml) and dichloromethane (500 ml). The layers were separated, and the organic phase was dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel using an elution gradient of toluene:ethyl acetate (100:0 to 96:4) to afford the title compound, 1.78 g. 1H-NMR (CDCl3, 400 MHz) δ: 0.98 (m, 2H), 1.20 (m, 4H), 1.68 (m, 7H), 4.00 (t, 2H), 7.4 (s, 1H), 7.60 (s, 1H), 9.80 (s, 1H). LRMS: m/z (TSP+) 207.2 [MH+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713496B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-33dff91b72c14abda21f5070743bc992
출처 메모uspto-grants-2004_03