HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370283Generated: October 26, 2026
Water → Ethyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/370283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Piperazinecarboxylic acid, ethyl ester | HCID 8431 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-(2-Chloroethoxy)acetamide | HCID 11018931 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Ethyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate | HCID 21188378 | 82.3% |
Reaction Steps
15.13 g of (2-chloroethoxy)acetamide (0.11 mol), 14.6 ml of ethyl piperazine carboxylate (0.1 mol), 23.3 g of sodium carbonate (0.22 mol) and 1.0 g of potassium iodide in 25 ml of toluene are introduced into a round-bottomed flask fitted with a water-cooled condenser and a mechanical stirrer. The mixture is heated at the reflux temperature for 4 hours and is allowed to cool to room temperature. The reaction is continued, still with stirring, for a further 16 hours. 100 ml of isopropanol are added and the solid materials formed are filtered off. The solvent is evaporated from the filtrate under reduced pressure to dryness. The product obtained after evaporation of the solvents is recrystallized from toluene. 21.35 g of ethyl 4-(2-carbamoylmethoxyethyl)piperazine-1-carboxylate are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140501 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-b24ca0e6cd364448a79b8afced73a8f9 |
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| Source note | uspto-grants-2000_10 |
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