HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274909Generated: October 30, 2026
Phenethylamine → 1-{4-[4,4-Bis(4-fluorophenyl)butyl]piperazin-1-yl}-3-[(2-phenylethyl)amino]propan-2-ol
https://huagongshe.com/reaction/274909
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[4,4-Bis(4-fluorophenyl)butyl]-4-[(oxiran-2-yl)methyl]piperazine | HCID 20088935 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{4-[4,4-Bis(4-fluorophenyl)butyl]piperazin-1-yl}-3-[(2-phenylethyl)amino]propan-2-ol | HCID 3072703 | 9.8% |
Reaction Steps
3.86 g (0.01 mol) of 1-[4,4-bis(4-fluorophenyl)butyl]-4-(2,3-epoxypropyl)piperazine and 1.2 g (0.01 mol) of 2-phenylethylamine were refluxed with heating together with 200 ml of DMF for 24 hours in the presence of a catalytic amount of an alkali such as potassium carbonate. DMF was distilled off under reduced pressure, and a residue was extracted with ethyl acetate. After washing with water and drying, the ethyl acetate was distilled off under reduced pressure to obtain 5 g of a crude subject compound of a viscous liquid. The obtained compound was refined by flush chromatography and fractional thin-layer chromatography with solvent mixtures of ethyl acetate--methanol and methylene chloride--methanol respectively to obtain 0.5 g of the subject compound in a viscous liquid state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391552 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-b3bc8119afd54343b061758f78adb9a0 |
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| Source note | uspto-grants-1995_02 |
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