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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431717Generated: October 26, 2026

4-(Diethylamino)benzaldehyde → HCID 178463809, compound

https://huagongshe.com/reaction/431717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Diethylamino)benzaldehydeHCID 67114—
Reactant3,5-Diamino-2-methylbenzoic acidHCID 135524—
SolventNitrobenzeneHCID 7416—
ProductHCID 178463809HCID 17846380982%

Reaction Conditions

Temperature145 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660742B2
Source datasetuspto-grants-2003_12
ORD IDord-468ef4aa63f642c78e6e003b0413293d
Source noteuspto-grants-2003_12