HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648658Generated: October 30, 2026
Hydrochloric Acid → 2-(Fluoromethyl)piperazine dihydrochloride
https://huagongshe.com/reaction/1648658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dibenzyl-2-(fluoromethyl)piperazine | HCID 14479499 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(Fluoromethyl)piperazine dihydrochloride | HCID 14479502 | — |
Reaction Steps
A mixture of a solution of 23.85 g (0.08 mole) of 1,4-dibenzyl-2-fluoromethylpiperazine [prepared as described in step (c) above] in 500 ml of methanol and 33 ml of concentrated aqueous hydrochloric acid was stirred vigorously at room temperature for 1 hour in an atmosphere of hydrogen and in the presence of 1.0 g of 20% w/w palladium-on-carbon. At the end of this time, the catalyst was removed by filtration and washed with water. The filtrate and washings were concentrated by evaporation under reduced pressure, and the residue was dissolved in 200 ml of water. The resulting aqueous solution was washed vigorously with ethyl acetate and separated. The aqueous layer was concentrated by evaporation under reduced pressure, and the residue was washed with ethanol to afford 13.76 g of 2-fluoromethylpiperazine dihydrochloride as a colorless powder, melting at 205°-218° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436367 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-c221cfdebc9c4161b9bc59561ff48598 |
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| Source note | uspto-grants-1995_07 |
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