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HRID 433647作成日:2026年10月25日

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

https://huagongshe.com/reaction/433647

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物(1-methyl-1H-imidazol-2-yl)methanolHCID 573612—
溶媒TetrahydrofuranHCID 8028—
生成物(5-bromo-1-methyl-1H-imidazol-2-yl)methanolHCID 2344517167%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06667335B2
出典データセットuspto-grants-2003_12
ORD IDord-4d417752ae244f4f93c0d0ff86060e71
出典メモuspto-grants-2003_12