HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361440Generated: October 25, 2026
Piperazine → 1-(2-Chloro-4-fluorophenyl)piperazine
https://huagongshe.com/reaction/1361440
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 1-Bromo-2-chloro-4-fluorobenzene | HCID 2733406 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2-Chloro-4-fluorophenyl)piperazine | HCID 18423151 | — |
Reaction Steps
A suspension of 1-bromo-2-chloro-4-fluorobenzene (4.19 g, 20 mmoles), piperazine (10.32 g, 120 mmoles), sodium tert-butoxide (2.3 g, 1.5 mmoles), tris(dibenzylideneacetone)dipalladium (366 mg, 0.4 mmoles) and racemic (−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (747 mg, 1.2 mmoles) in toluene (2 mL) was heated to 120° C. overnight. The mixture was cooled, filtered and the filtrate concentrated under reduced pressure. The crude residue was purified by column chromatography (silica gel, 0-5% 2N methanolic ammonia in DCM) to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07880001B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-ddc7e461a1fe4f839bf012a6fe8b1db8 |
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| Source note | uspto-grants-2011_02 |
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