Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6431Erstellt: 23. Oktober 2026

O-Phenylenediamine → 2-(1H-Pyrrol-2-yl)-1H-benzimidazole

https://huagongshe.com/de/reaction/6431

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-PhenylenediamineHCID 7243—
EduktPyrrole-2-Carboxylic AcidHCID 12473—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt2-(1H-Pyrrol-2-yl)-1H-benzimidazoleHCID 63941927,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1.08 g (10 mmol) of o-phenylenediamine and 20 g of polyophosphate esters was heated gently at 80° C. and was added portionwise 1.11 g (10 mmol) of pyrrole-2-carboxylic acid. After the mixture was stirred at 100° C. for 30 minutes, it was poured into a saturated solution of sodium bicarbonate (500 mL) and stirred until polyphosphate esters was decomposed. It was then extracted with two 400 mL portions of ethyl acetate. the separated organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a crude product. After purification by column chromatography on silica gel with 30% ethyl acetate in hexane, the desired product, 2-(pyrrol-2-yl)benzimidazole (0.50 g, 25%) was obtained as a pale yellow solid, m.p. 250° C.; 1H-NMR (Acetone-d6) 6.25-6.27 (m, 1H, ArH), 6.90-6.92 (m, 1H, ArH), 7.02-7.03 (m, 1H, ArH), 7.14-7.19 (m, 2H, 2xArH), 7.52 (bs, 2H, 2xArH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05248782
Quelldatensatzuspto-grants-1993_09
ORD IDord-f133d8b34fb84de6ae33d093fc5b41e4
Quellennotizuspto-grants-1993_09