HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395247Generated: November 2, 2026
Acetone → 2-(4-Ethylpiperazin-1-yl)ethan-1-amine
https://huagongshe.com/reaction/2395247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 1-(2-Hydroxyethyl)piperazine | HCID 7677 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Product | 2-(4-Ethylpiperazin-1-yl)ethan-1-amine | HCID 776622 | 41% |
Reaction Steps
To a solution of 1-piperazineethanol(2.28 g) in acetone(40 ml) were added bromoacetonitrile(2.40 g) and potassium carbonate(5.53 g) and then the mixture was stirred at room temperature for 4 hours. After the reaction, the reaction mixture was washed with saturated brine and water successively, dried over sodium sulfate anhydride, and concentrated under a vacuum. To the residue dissolved in methanol(60 ml) were added cobalt chloride(9.50 g) and sodium borohydride(7.60 g), and then the mixture was stirred at room temperature for 30 minutes. After the reaction mixture was concentrated, the resulting residue was dissolved in chloroform. After a filtration, the filtrate was concentrated, thereby yielding 1.17 g (41%) of 4-(2-aminoethyl)-1-ethylpiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05814634 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-c726af1a0cf840eb8f44d7f777dd25ed |
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| Source note | uspto-grants-1998_09 |
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