HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4314Generated: October 25, 2026
Ethanol → 1-(4-Fluorobenzyl)piperazine
https://huagongshe.com/reaction/4314
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 4-Fluorobenzyl chloride | HCID 9602 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(4-Fluorobenzyl)piperazine | HCID 796563 | 55.7% |
Reaction Steps
A solution of 29 g of p-fluorobenzyl chloride in 50 g of reagent ethanol was added dropwise to a stirred solution of 34.5 g of piperazine in 150 g of reagent ethanol. A cold water bath was used to maintain the reaction temperature at 20° C. during the addition. The reaction mixture was stirred for an additional 11/2 hours and then added to 2 liters of ether. Precipitated piperazine hydrochloride was filtered off. The filtrate was concentrated to an oil, which was chromatographed on a silica column, the eluant being a mixture of CH2Cl2 /methanol/ammonium hydroxide in the ratio of 45:5:1. After concentration of appropriate fractions, 21.7 g of 1-(4-fluorobenzyl)piperazine were isolated as a colorless liquid (56% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04725597 |
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| Source dataset | uspto-grants-1988_02 |
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| ORD ID | ord-3ac68fcac968481094ca4e6ef976f341 |
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| Source note | uspto-grants-1988_02 |
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