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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1376364Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1376364

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,5-TriphenylimidazoleHCID 10232—
EduktPotassium HydroxideHCID 14797—
EduktSodium hydrideHCID 24758—
EduktMethyl 7-bromohept-5-ynoateHCID 11287432—
LösungsmittelMethanolHCID 887—
Produkt7-(1,2,4-Triphenyl-imidazolyl)-hept-5-ynoic acidHCID 53688979—

Reaktionsschritte

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%

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05663053
Quelldatensatzuspto-grants-1997_09
ORD IDord-5267751af1ed4384aa2f4197c04d07a6
Quellennotizuspto-grants-1997_09