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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1376364생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1376364

반응식

참여 물질

역할이름HCID투입량
반응물2,4,5-TriphenylimidazoleHCID 10232—
반응물Potassium HydroxideHCID 14797—
반응물Sodium hydrideHCID 24758—
반응물Methyl 7-bromohept-5-ynoateHCID 11287432—
용매MethanolHCID 887—
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-formimide (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 번호US05663053
출처 데이터셋uspto-grants-1997_09
ORD IDord-5267751af1ed4384aa2f4197c04d07a6
출처 메모uspto-grants-1997_09