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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431717Erstellt: 27. Oktober 2026

4-(Diethylamino)benzaldehyde → HCID 178463809, Verbindung

https://huagongshe.com/reaction/431717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Diethylamino)benzaldehydeHCID 67114—
Edukt3,5-Diamino-2-methylbenzoic acidHCID 135524—
LösungsmittelNitrobenzeneHCID 7416—
ProduktHCID 178463809HCID 17846380982%

Reaktionsbedingungen

Temperatur145 °C

Reaktionsschritte

Methyl 3,4-diaminobenzoate (0.73 g, 4.42 mmol), 4-(diethylamino)benzaldehyde (3.0 g, 16.9 mmol) were dissolved in nitrobenzene (30 mL) and refluxed on a 145° C. oil bath overnight. The nitrobenzene was then removed in vacuo using a Kugelrohr apparatus (60° C., 0.1 mm Hg). The remaining oily residue was dissolved in CHCl3 and washed with water (3×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated. The crude oil was then purified through colurnn chromatography using a solvent system of 1% MeOH/CHCl3 to give methyl 2-(4-(N,N-diethyl)aminophenyl)benzimidazole-6-carboxylate as a yellowish solid (1.17 g, 82% yield). TLC (2.5% MeOH/CHCl3) Rf=0.26; 1H-NMR (500 MHz, CDCl3) 9.87 (s br, 1H), 8.30 (s br, 1H), 7.94 (dd, 1.5, 8.5, 1H), 7.91 (d, 8.5, 2H), 7.60 (s br, 1H), 6.72 (d, 8.5, 2H), 3.42 (q, 7.0, 4H), 1.21 (t, 7.0, 6H); IR (neat) 3508, 2063, 2920, 1712, 1611, 1504, 1434, 1360, 1307, 1269, 1205, 1157, 1082, 1008, 821, 751.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660742B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-468ef4aa63f642c78e6e003b0413293d
Quellennotizuspto-grants-2003_12