HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003320Generated: October 31, 2026
Piperazine → 1-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-one
https://huagongshe.com/reaction/1003320
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[4-(Propan-2-yl)piperazin-1-yl]ethan-1-one | HCID 18796419 | — |
Reaction Steps
To 12.95 g of piperazine, 0.75 g of sodium iodide and 3.46 g of potassium carbonate were added successively 25 ml of methanol and 6.15 g of 2-bromopropane and the mixture was stirred at 60° C. for 4 hours. After the addition of chloroform and washing with a saturated aqueous solution of sodium chloride, the mixture was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, 12 ml of acetic anhydride was slowly added and the mixture was stirred at room temperature for 2.5 hours. The reaction solution was poured into ice and chloroform was added and the mixture was neutralized with sodium carbonate. After extracting with chloroform, the extract was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue thus obtained was chromatographed over a silica gel column. The solvent was distilled off and the residue was allowed to stand overnight. The diacetylpiperazine thus precipitated out was filtered off to afford 7.26 g of the title compound as an oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046201 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-ab004de9e77242eeaf0b66d58115bfd2 |
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| Source note | uspto-grants-2000_04 |
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