HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916481Generated: October 29, 2026
2-Bromoethanol → 2-[4-(2-Fluoroethyl)piperazin-1-YL]ethanol
https://huagongshe.com/reaction/916481
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethanol, 1-bromo- | HCID 14202443 | — |
| Reactant | HCID 87238377 | HCID 87238377 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-(2-Fluoroethyl)piperazin-1-YL]ethanol | HCID 45099649 | 66.4% |
Reaction Steps
1-(2-Fluoroethyl)piperazine diTFA salt (464 mg, 1.29 mmol), (prepared as described for the starting material in Example 27), was dissolved in acetonitrile (3.5 ml). Potassium carbonate (889 mg, 6.44 mmol) and 2-bromoethanol (95 μl, 1.34 mmol) were added and the mixture heated to 85° C. and left overnight. More bromoethanol (95 μl, 1.34 mmol) was added and the reaction mixture heated at 85° C. for a further 2 hours. The reaction mixture was cooled, filtered and concentrated. The residue was purified by column chromatography eluting with methylene chloride/methanol (saturated with ammonia) (92/8) to give 2-[4-(2-fluoroethyl)piperazin-1-yl]ethanol (151 mg, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268230B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-8ef5f226b33742daa00b5744de1794bc |
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| Source note | uspto-grants-2007_09 |
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