Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1719388Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1-(p-Carboxybenzyl)-2-(1-imidazolyl)-3-methylindole

https://huagongshe.com/reaction/1719388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt2-(Bromomethyl)benzoic acidHCID 346003—
Edukt2-(1-Imidazolyl)-3-methylindoleHCID 13280839—
LösungsmittelWaterHCID 962—
Produkt1-(p-Carboxybenzyl)-2-(1-imidazolyl)-3-methylindoleHCID 13491436—

Reaktionsschritte

A solution of 3-methyl-2-(1-imidazolyl)indole (1.50 g) in dimethylformamide (10 ml) is added dropwise to a suspension of 50% sodium hydride dispersion in mineral oil (0.77 g) in dimethylformamide (20 ml) stirred under nitrogen at 5°-10°. The suspension is stirred at 5°-10° for 1/2 hour. A solution of α-bromotoluic acid (1.63 g) in dimethylformamide (5 ml) is added dropwise to the suspension. The suspension is again stirred at 5°-10° for 1/2 hour and then overnight at room temperature. The suspension is diluted with water (100 ml) and acidified to pH 6 to 7 with 1N hydrochloric acid. The white precipitate which forms is collected by vacuum filtration, washed with water and dried to give 1-(p-carboxybenzyl)-2-(1-imidazolyl)-3-methylindole, m.p. 221°-5°. Recrystallization from acetonitrile gives crystals melting at 225°-7°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04539410
Quelldatensatzuspto-grants-1985_09
ORD IDord-64ee2ada45f34c5985bbb6b866e2ac32
Quellennotizuspto-grants-1985_09