Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 973418Erstellt: 24. Oktober 2026

O-Phenylenediamine → 2-(1-Methyl-3-pyrrolidinyl)-1H-benzimidazole

https://huagongshe.com/de/reaction/973418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-PhenylenediamineHCID 7243—
EduktAmmonium HydroxideHCID 14923—
Edukt1-Methylpyrrolidine-3-carbonitrileHCID 10866285—
LösungsmittelHydrochloric AcidHCID 313—
Produkt2-(1-Methyl-3-pyrrolidinyl)-1H-benzimidazoleHCID 19989862—

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

To 240 g of concentrated hydrochloric acid was added 43.2 g (0.39 mol) of 3-cyano-1-methylpyrrolidine (the temperature rose to 90° C.). After the temperature began to fall the solution was heated to 110° C. for 4 h. The solution was cooled to 60° C. and 42 g (0.39 mol) of 1,2-diaminobenzene in 250 mL of 1N hydrochloric acid was added. The solution was heated to reflux for 20 h. The cooled solution was made basic with concentrated NH4OH and the resulting crystals were collected by filtration. The product was chromatographed on a 7.5×36 cm silica column eluting with 1 gallon of 10% NH4OH-90% ethanol. The eluent was collected in 500-mL portions. The first 6 fractions were discarded and fractions 7-14 were collected and concentrated. The residue was recrystallized from ethyl acetate. Yield: 18 g (23%). A 5-g sample was recrystallized three times from ethyl acetate. Yield: 1.6 g, mp 189°-193° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05063228
Quelldatensatzuspto-grants-1991_11
ORD IDord-4825ff80ed504d4eac904674a4287a2c
Quellennotizuspto-grants-1991_11