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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 653932생성일: 2026년 10월 25일

Tetrahydrofuran → 1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazole

https://huagongshe.com/reaction/653932

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물2-Butyl-5-chloro-3-(4-nitro-benzyl)-3h-imidazole-4-carbaldehydeHCID 19815397—
반응물ButyllithiumHCID 178418339—
촉매Benzyltriphenylphosphonium chlorideHCID 70671—
생성물1-(4-Nitrobenzyl)-2-butyl-4-chloro-5-(2-phenylethen-1-yl)imidazoleHCID 54113661—

반응 단계

A solution of 0.4 g of benzyltriphenylphosphonium chloride in 20 ml of dried THF was cooled to -30°. To the above solution was added 0.65 mL of 1.6 M n-BuLi dropwise. As the BuLi was added the solution turned to deep orange color. After stirring for 10 min. at -30°, 0.32 g of 1-(4-nitrobenzyl)-2-butyl-4-chloroimidazole-5-aldehyde was added and the reaction mixture was allowed to warm up to room temperature and stirred at room temperature for 2 hours. The reaction mixture was quenched with 2 mL of saturated NH4Cl solution and diluted with ethyl acetate, and the ethyl acetate solution was washed with water and a brine solution. Evaporation gave a thick oil residue which was purified by the flash silica gel column chromatography (hexane:ethyl acetate=3:1 elution) to give a thick yellow oil, 0.39 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05128355
출처 데이터셋uspto-grants-1992_07
ORD IDord-0e9fa32cf7744476a03699f607183bfc
출처 메모uspto-grants-1992_07