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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1032327생성일: 2026년 10월 25일

Imidazole → 3-[(1H-imidazol-1-yl)methyl]-1,2-benzisoxazole

https://huagongshe.com/reaction/1032327

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물1,2-Benzisoxazole, 3-(bromomethyl)-HCID 3499189—
용매DimethylformamideHCID 6228—
용매HexaneHCID 8058—
생성물3-[(1H-imidazol-1-yl)methyl]-1,2-benzisoxazoleHCID 14575002—

반응 조건

온도85 °C

반응 단계

Sodium hydride (50% in mineral oil, 3.4 g, 0.071 mole) is washed free of mineral oil with hexane (3×30 mL) and suspended in dimethylformamide (100 mL). This suspension is well stirred and maintained near room temperature (water bath) during the dropwise addition of a solution of imidazole (4.8 g, 0.071 mole) in dimethylformamide (25 mL). The reaction mixture is stirred at room temperature for 1 hour when 3-bromomethyl-1,2-benzisoxazole (15.0 g, 0.071 mole) is added all at once. The mixture is then heated at 85° C. for 8 hours. The solvent is evaporated in vacuo and the residue is taken up in methylene chloride (200 mL) and washed with water (3×50 mL). The organic solution is dried over anhydrous sodium sulfate, filtered and evaporated to give 3-[(1H-imidazol-1-yl)methyl]-1,2-benzisoxazole, which is purified by recrystallisation from isopropanol, m.p. 52-55° C. The free base is converted to the hydrochloride salt m.p. 145-146° C., when its solution in isopropanol is treated with a small excess of ethereal hydrogen chloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04957931
출처 데이터셋uspto-grants-1990_09
ORD IDord-202d7386ca9c4d8ab7768b44b259af98
출처 메모uspto-grants-1990_09