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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265390생성일: 2026년 10월 26일

2,4,5-Triphenylimidazole → 7-(1,2,4-Triphenyl-imidazolyl)-hept-5-ynoic acid

https://huagongshe.com/reaction/265390

반응식

참여 물질

역할이름HCID투입량
반응물2,4,5-TriphenylimidazoleHCID 10232—
반응물Potassium HydroxideHCID 14797—
반응물Sodium hydrideHCID 24758—
반응물Methyl 7-bromohept-5-ynoateHCID 11287432—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물7-(1,2,4-Triphenyl-imidazolyl)-hept-5-ynoic acidHCID 53688979—

반응 단계

A solution of 2,4,5-triphenylimidazole (1.07 g) in dimethyl-formamide (20 ml) was treated with sodium hydride 50% in oil (0.17 g) and methyl 7-bromohept-5-ynoate (0.95 g). The solution was stirred for 18 hours when the solvent was removed under reduced pressure and the residue was chromatographed on silica gel eluted with chloroform-hexane to give a clear oil which was dissolved in methanol (20 ml) and treated with 10% potassium hydroxide solution (10 ml) for 2 hours. The methanol was removed under reduced pressure and the remaining aqueous was acidified (pH 3) and filtered. The filtrate was extracted with chloroform (3×50 ml). The chloroform extracts were dried over magnesium sulphate, filtered and the solvent removed to give a solid which was recrystallised from acetonitrile to give 7-(1,2,4-triphenyl-imidazolyl)-hept-5-ynoic acid as white prisms, m.p. 144°-145° C.; Found: C, 79.99; H, 5.81; N, 6.40% (C28H24N2O2);Requires: C, 79.97; H, 5.75; N, 6.66%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648373
출처 데이터셋uspto-grants-1997_07
ORD IDord-31e89f06d4824217bc472c262f066c8c
출처 메모uspto-grants-1997_07