Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358143Generated: October 30, 2026

Triethylamine → 2-{[(4-Nitrophenyl)methyl]amino}propanediamide

https://huagongshe.com/reaction/358143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-NitrobenzylamineHCID 29147—
Reactant2-BromopropanediamideHCID 13271628—
SolventEthanolHCID 702—
Product2-{[(4-Nitrophenyl)methyl]amino}propanediamideHCID 1327162977.6%

Reaction Steps

To a solution of 41.60 g of p-nitrobenzylamine in 660 ml of dry ethanol was added 49.34 g of α-bromomalonamide and 38.2 ml of triethylamine. After being stirred for two hours under refluxing, the reaction mixture was cooled to room temperature. And then separated crystals were filtered off, washed with ethanol and isopropyl ether, and dried to give 53.36 g of α-(4-nitrobenzyl)aminomalonamide. And a mixture of 50.45 g of α-(4-nitrobenzyl)aminomalonamide, 177.8 g of triethyl orthoformate and 0.76 g of p-toluenesulfonic acid monohydrate in 1.3 liters of dry ethanol was stirred for three hours under refluxing in an argon atmosphere. The reaction mixture was cooled on an ice-bath and separated crystals were filtered off, washed with ethanol and isopropyl ether, and dried to give 50.78 g of 5-carbamoyl-1-(4-nitrobenzyl)imidazolium-4-olate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04464531
Source datasetuspto-grants-1984_08
ORD IDord-98464c4a2da844be94b5099d8adaa04f
Source noteuspto-grants-1984_08