HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182210Generated: October 31, 2026
Bromide ion → 1-(2,4-Difluorophenyl)piperazine
https://huagongshe.com/reaction/2182210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1-Bromo-2,4-difluorobenzene | HCID 67674 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(2,4-Difluorophenyl)piperazine | HCID 2734637 | — |
Reaction Steps
1-(2,4-Difluorophenyl)piperazine is prepared from 2,4-difluorobromobenzene. To the bromide (8.0 g, 41.4 mmol), piperazine (21.4 g, 249 mmol), sodium t-butoxide (5.6 g, 58 mmol) and BINAP (1.55 g, 2.5 mmol) in toluene (20 ml), add Pd2(dba)3 (0.477 g, 0.83 mmol). Heat the mixture at 110° C. under N2 for 20 h. Allow to cool and extract with 1N HCl. Basify the extract with NaOH to pH=10, extract with CH2Cl2, dry and concentrate to obtain the title compound as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06897216B2 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-8ce9e0a259f642faa81042a406532774 |
|---|
| Source note | uspto-grants-2005_05 |
|---|