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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763530Generated: October 30, 2026

Methyl iodide → HCID 20483275, compound

https://huagongshe.com/reaction/1763530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15582243HCID 15582243—
SolventDimethylformamideHCID 6228—
ProductHCID 20483275HCID 20483275—

Reaction Steps

To a solution of 6.4 g of 1-formyl-3-oxo-piperazine in 10 ml of anhydrous dimethylformamide was added 2.7 g of a sodium hydride (purity 53%) with ice-cooling, and the resulting mixture was reacted at room temperature for 1 hour. Subsequently, the mixture was incorporated with 7.1 g of methyl iodide and reacted for 10 hours. After the reaction, the dimethylformamide was removed by reduced pressure distillation to obtain 1-formyl-4-methyl-3-oxo-piperazine. This piperazine was dissolved in 70 ml of a 50% aqueous acetone solution containing 2.2 g of sodium hydroxide, and the resulting solution was reacted at room temperature for 3 hours. Thereafter, the solvent was removed by distillation under reduced pressure, and the residue was charged into acetone to deposit insolubles. The insolubles were separated by filtration, and the acetone was removed from the filtrate by distillation under reduced pressure. Subsequently, the residue was subjected to reduced pressure distillation to obtain 5.2 g of 1-methyl-2-oxo-piperazine, b.p. 104° C/4 mmHg, yield 91%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112090
Source datasetuspto-grants-1978_09
ORD IDord-61d69c4f901c470faa064b503786d477
Source noteuspto-grants-1978_09