HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440113Generated: October 29, 2026
Benzylamine → 1,4-Dibenzyl-2-(fluoromethyl)piperazine
https://huagongshe.com/reaction/1440113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(3-fluoro-2-methylsulfonyloxypropyl)-N-(2-methylsulfonyloxyethyl)benzylamine | HCID 18985366 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,4-Dibenzyl-2-(fluoromethyl)piperazine | HCID 14479499 | — |
Reaction Steps
4.82 g (0.045 mole) of benzylamine and 9.09 g (0.09 mole) of triethylamine were added to a solution of N-(3-fluoro-2-methylsulfonyloxypropyl)-N-(2-methylsulfonyloxyethyl)benzylamine [prepared as described in step (b) above] dissolved in 200 ml of ethanol. The mixture was heated under reflux for 2 hours and then concentrated by evaporation under reduced pressure. 100 ml of ethanol and 40 ml of a 2N aqueous solution of sodium hydroxide were added to the residue, and the mixture was concentrated by evaporation under reduced pressure. The residue was mixed with ethyl acetate, and insoluble materials were removed by filtration. The filtrate was freed from the solvent by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 3.60 g of 1,4-dibenzyl-2-fluoromethylpiperazine as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05496951 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-2f79ce83854b406396315b7bc43d47b6 |
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| Source note | uspto-grants-1996_03 |
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