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HRID 523042作成日:2026年10月26日

N-bromobutanimide → HCID 178470399、化合物

https://huagongshe.com/reaction/523042

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Ethyl 4(5)-imidazolecarboxylateHCID 99170—
溶媒AcetonitrileHCID 6342—
生成物HCID 178470399HCID 178470399—

反応手順

NBS (25 g, 140 mmol) is added to a stirred solution of ethyl 3H-imidazole-4-carboxylate (I-17) in 1.4 L of MeCN. The reaction mixture is stirred for 12 h in the dark, then is concentrated and purified by silica chromatography (0-70% EtOAc in heptane) to provide 17 g (65 mmol) of ethyl 3H-imidazole-4-carboxylate ethyl 4-bromo-1H-imidazole-5-carboxylate (I-18) as a white solid. This material is stirred with 11 g (78 mmol) of K2CO3 and 8.5 mL (71 mmol) of benzyl bromide in 200 mL of DMF for 12 h. The reaction is diluted with water and extracted with three times with EtOAc. Extracts are combined, washed with brine, dried over Na2SO4, filtered, concentrated and purified via silica chromatography (0-50% EtOAc in heptane) to provide 9.6 g (31 mmol) of ethyl 3-benzyl-5-bromo-imidazole-4-carboxylate (I-19) as a colorless oil that solidified upon standing.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334285B2
出典データセットuspto-grants-2016_05
ORD IDord-6f9834d4244a4299a27c518716e7e373
出典メモuspto-grants-2016_05