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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501390생성일: 2026년 10월 26일

Ethanol → Ethyl 2-bromo-3-(2-butynyl)-5-cyano-3H-imidazole-4-carboxylate

https://huagongshe.com/reaction/501390

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sulfuric AcidHCID 1118—
반응물Ethyl AcetateHCID 8857—
반응물2-bromo-1H-imidazole-4,5-dicarbonitrileHCID 2779148—
용매WaterHCID 962—
생성물Ethyl 2-bromo-3-(2-butynyl)-5-cyano-3H-imidazole-4-carboxylateHCID 23070799—

반응 단계

4.56 ml of sulfuric acid was added to 170 ml of ethanol containing 16.80 g of 2-bromo-1H-imidazole-4,5-dicarbonitrile [CAS No. 50847-09-1], and the mixture was heated under reflux for 48 hours. The solution was cooled, and then 500 ml of ethyl acetate and 200 ml of water were added thereto. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was dissolved in N,N-dimethylformamide, and 14.1 g of potassium carbonate and 8.6 ml of 2-butynyl bromide were added thereto. The mixture was stirred at room temperature for 18 hours. 500 ml of ethyl acetate was added to the solution, and the mixture was washed three times with 300 ml of water, and then with 300 ml of a saturated sodium chloride solution. Then, the solution was dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography. Thus, 4.09 g of the title compound was obtained from the fraction eluted with hexane-ethyl acetate (9:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772226B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-ae898081371343318d97305860d4dc5d
출처 메모uspto-grants-2010_08