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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzylamine | HCID 29147 | — |
| Reactant | 2-Bromopropanediamide | HCID 13271628 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-{[(4-Nitrophenyl)methyl]amino}propanediamide | HCID 13271629 | 77.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464531 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-98464c4a2da844be94b5099d8adaa04f |
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| Source note | uspto-grants-1984_08 |
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