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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantVeratroyl chlorideHCID 77070—
Reactant2-Nitro-5-piperazinylbenzaldehydeHCID 10989384—
SolventDimethylformamideHCID 6228—
Product2-Nitro-5-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]benzaldehydeHCID 1323630153%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04415572
Source datasetuspto-grants-1983_11
ORD IDord-4d3ce01e8b304e919e6c0f6711038b89
Source noteuspto-grants-1983_11