HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649199Generated: October 31, 2026
Triethylamine → 2-Nitro-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]benzaldehyde
https://huagongshe.com/reaction/1649199
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Veratroyl chloride | HCID 77070 | — |
| Reactant | 2-Nitro-5-piperazinylbenzaldehyde | HCID 10989384 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Nitro-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]benzaldehyde | HCID 13236301 | 53% |
Reaction Steps
2-Nitro-5-piperazinylbenzaldehyde (5 g) was suspended in 50 ml of DMF and 6 ml of triethylamine was added to the suspension. A solution of 4.4 g of 3,4-dimethoxybenzoyl chloride in 20 ml of DMF was added dropwise thereto with ice cooling externally while stirring and the mixture was stirred at room temperature for 2 hours and poured into saturated saline and extracted with methylene chloride. After washing with water, the methylene chloride layer was dried over anhydrous sodium sulfate. Then, the solvent was removed by distillation and to the residue was added methyl alcohol and the mixture was heated and cooled and crystals which formed were recrystallized form DMF to give 4.5 g of 2-nitro-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]benzaldehyde, m.p. 196°-198° C., yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04415572 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-4d3ce01e8b304e919e6c0f6711038b89 |
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| Source note | uspto-grants-1983_11 |
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