HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358111Generated: October 26, 2026
Piperazine → 1-(2-Fluoro-3-(trifluoromethyl)phenyl)piperazine
https://huagongshe.com/reaction/2358111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 3-Bromo-2-fluorobenzotrifluoride | HCID 2736320 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | (+-)-1,1'-Binaphthyl-2,2'-diyl hydrogen phosphate | HCID 99589 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Fluoro-3-(trifluoromethyl)phenyl)piperazine | HCID 57448041 | 54.5% |
Reaction Steps
To a solution of 3-bromo-2-fluorobenzotrifluoride (1.72 g, 7.1 mmol) in toluene (50 ml) under nitrogen, was added piperazine (0.89 g, 10.6 mmol), potassium tert-butoxide (0.95 g, 9.9 mmol), bis(dibenzylideneacetone)palladium(0) (0.19 g, 0.21 mmol) and (+/−)-1,1′-binaphthyl-2,2′-diyl hydrogen phosphate (0.13 g, 0.21 mmol). The resulting mixture was heated at 80° C. for 20 h. Filtration through a pad of celite and evaporation of the filtrate gave 2.1 g of crude product. The residue was purified by flash column chromatography (ethylacetate/methanol, 1:1) to give the title compound (0.96 g). MS m/z (rel. intensity, 70 eV) 248 (M+, 23), 207 (10), 206 (bp), 190 (17), 163 (8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763639B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-d63c18f880834a3c8157445c1ac37136 |
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| Source note | uspto-grants-2010_07 |
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