HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622453Generated: October 30, 2026
Sodium Chloride → Tert-butyl 4-methyl-3-oxopiperazine-1-carboxylate
https://huagongshe.com/reaction/622453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-methyl-3-oxopiperazine-1-carboxylate | HCID 18783916 | — |
Reaction Steps
8 g of 4-t-butoxycarbonyl-2-oxopiperazine (previously prepared from 2-oxopiperazine and di-t-butyl dicarbonate) were dissolved in 80 ml of dimethylformamide. 1.92 g of sodium hydride (55%, in paraffin) were added to this solution, and the mixture was stirred at room temperature for one hour. A solution of 6.8 g of methyl iodide in 20 ml of dimethylformamide was then added, and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was then poured into a saturated aqueous solution of sodium chloride and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography through silica gel, eluted with ethyl acetate, to give 3.0 g of 1-methyl-2-oxo-4-t-butoxycarbonylpiperazine in the form of colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04771046 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-f25312bea45241829181cc6fa674b465 |
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| Source note | uspto-grants-1988_09 |
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