HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431717Generated: October 26, 2026
4-(Diethylamino)benzaldehyde → HCID 178463809, compound
https://huagongshe.com/reaction/431717
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Diethylamino)benzaldehyde | HCID 67114 | — |
| Reactant | 3,5-Diamino-2-methylbenzoic acid | HCID 135524 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 178463809 | HCID 178463809 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06660742B2 |
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| Source dataset | uspto-grants-2003_12 |
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| ORD ID | ord-468ef4aa63f642c78e6e003b0413293d |
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| Source note | uspto-grants-2003_12 |
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