HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657604Generated: October 27, 2026
Methyl iodide → 3,3,4-Trimethylpiperazin-2-one
https://huagongshe.com/reaction/657604
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Piperazinone, 3,3-dimethyl- | HCID 211157 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3,3,4-Trimethylpiperazin-2-one | HCID 20310182 | 73.9% |
Reaction Steps
3,3-dimethylpiperazin-2-one (50 grams) is suspended in 1,2-dimethoxyethane (DME) (150 ml) and potassium carbonate (70 grams) is added. Methyl iodide (66.4 grams) is added during half an hour, while the mixture is cooled slightly, allowing the temperature to reach 50° C. The mixture is stirred 9 hours at an oil bath at 40-45° C., and a sample is withdrawn for NMR, which indicates, that there is still 8% starting material left (singal at 2.8 ppm). More methyl iodide is added (4.6 grams), and the mixture is stirred for another 2½ hour at 40° C., and a new NMR sample shows full conversion. The mixture is filtered, and the filter cake is washed with DME. The filtrate is evaporated to dryness giving 41 grams of the title compound. NMR complies with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076342B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-aee93ff20d1c4685ac0aa38b92d1abc2 |
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| Source note | uspto-grants-2011_12 |
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