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HRID 526838作成日:2026年10月27日

5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone

https://huagongshe.com/reaction/526838

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
反応物N-methoxy-N-methyl-4-nitrobenzamideHCID 2991007—
反応物HCID 178418443HCID 178418443—
溶媒DichloromethaneHCID 6344—
生成物(1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanoneHCID 86715600—

反応手順

To a solution of 5-bromo-1-methyl-1H-imidazole (3.22 g, 19.98 mmol) in DCM (15 mL) was added ethyl magnesium bromide (6.66 mL, 19.98 mmol, 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting orange-red solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methyl-4-nitrobenzamide (3.5 g, 16.65 mmol, Intermediate 7: step a) dissolved in DCM (10 mL) was added dropwise. The ice bath was removed and the solid suspension stirred at room temperature for 48 hours. Water was added followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346782B2
出典データセットuspto-grants-2016_05
ORD IDord-b41eba38d3cc48979088abf09e668c45
出典メモuspto-grants-2016_05