Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1419123Erstellt: 27. Oktober 2026

Benzyl Bromide → Methyl 1-benzyl-1H-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/1419123

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktPotassium CarbonateHCID 11430—
Eduktmethyl 1H-1,3-benzodiazole-5-carboxylateHCID 2779733—
LösungsmittelAcetoneHCID 180—
ProduktMethyl 1-benzyl-1H-benzimidazole-5-carboxylateHCID 5445048822,2%

Reaktionsschritte

A mixture of 2.8 g of methyl 5-benzimidazolecarboxylate (prepared as described in Preparation 26), 3.52 g of benzyl bromide, 3 g of potassium carbonate and 50 ml of acetone was stirred for 3 days at room temperature. At the end of this time, the solvent was removed by evaporation under reduced pressure and the residue was mixed with an aqueous solution of sodium chloride, after which it was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was then recrystallized from a mixture of ethyl acetate and hexane, to give 0.94 g of the title compound, melting at 156°-162° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05886014
Quelldatensatzuspto-grants-1999_03
ORD IDord-ba3e220a895f48f4abeccf9969b9d70b
Quellennotizuspto-grants-1999_03