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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantPiperazin-2-oneHCID 231360—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-methyl-3-oxopiperazine-1-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04771046
Source datasetuspto-grants-1988_09
ORD IDord-f25312bea45241829181cc6fa674b465
Source noteuspto-grants-1988_09