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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 526838생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/526838

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-1-methyl-1H-imidazoleHCID 1515258—
반응물N-methoxy-N-methyl-4-nitrobenzamideHCID 2991007—
반응물HCID 178418443HCID 178418443—
용매DichloromethaneHCID 6344—
생성물(1-Methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanoneHCID 86715600—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346782B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-b41eba38d3cc48979088abf09e668c45
출처 메모uspto-grants-2016_05