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HRID 928780作成日:2026年10月27日

5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanone

https://huagongshe.com/reaction/928780

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,3-dimethyl-4-nitrobenzamideHCID 46318653—
反応物HCID 178461630HCID 178461630—
溶媒DichloromethaneHCID 6344—
生成物(1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanoneHCID 86715615—

反応手順

A solution of EtMgBr (3.0 M in diethylether, 8.5 mL, 25.689 mmol) was added dropwise, over a 25 minutes period, to a solution of 5-bromo-1-methyl-1H-imidazole (4.1 g, 25.689 mmol) in dry DCM (25 mL). The mixture was stirred at room temperature for 15 minutes, cooled in an ice-brine bath and N-methoxy-N,3-dimethyl-4-nitrobenzamide (4.8 g, 21.408 mmol, Intermediate 40: step a) dissolved in 10 mL of DCM was added dropwise. A dark brown solid mass formed. The ice bath was removed and mixture stirred at room temperature for 48 hours. Water was added to the suspension followed by 6M aqueous HCl slowly to neutralize the mixture (pH=6-7). More DCM was added and layers separated. The organic layer was dried over Na2SO4, filtered and concentrated. Et2O was added, the slurry sonicated, and precipitates filtered 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US09290476B2
出典データセットuspto-grants-2016_03
ORD IDord-9a724315f22247e3bbcbfd7715bfbb9e
出典メモuspto-grants-2016_03