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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397950생성일: 2026년 10월 23일

N-bromobutanimide → (5-bromo-1-methyl-1H-imidazol-2-yl)methanol

https://huagongshe.com/ko/reaction/397950

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물(1-methyl-1H-imidazol-2-yl)methanolHCID 573612—
용매TetrahydrofuranHCID 8028—
생성물(5-bromo-1-methyl-1H-imidazol-2-yl)methanolHCID 2344517167%

반응 단계

1-Methylimidazole-2-methanol (3.15 g, 28 mmol) (R. J. Sundberg; P. V. Nguyen; Med. Chem. Res. 7, 2, 1997, 123-136) was suspensed in THF (75 ml) at −20° C. and treated slowly (within 30 min) with N-bromosuccinimide (4.9 g, 27 mmol). The reaction mixture was allowed to warm up slowly to room temperature and quenched with saturated aqueous NaHCO3 solution (50 ml). The aqueous layer was extracted 3 times with AcOEt. The combined extracts were washed with saturated aqueous NaHCO3 solution, dried over Na2SO4, filtered and the solvent was removed in vacuo. The residue was chromatographed (silica, elution first with AcOEt/hexane 1:1, then with CH2Cl2/MeOH 95:05) to provide the title compound (2.11 g, 67%) as a white solid. MS: m/e=191.2 (M+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06610723B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-8ad3e346f50746bc81bc84d5ea1bcb29
출처 메모uspto-grants-2003_08