HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888191Generated: October 27, 2026
4-Bromo-4'-fluoro-1,1'-biphenyl → HCID 58487952, compound
https://huagongshe.com/reaction/888191
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-4'-fluoro-1,1'-biphenyl | HCID 96882 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58487952 | HCID 58487952 | — |
Reaction Steps
A mixture of (R)-2-methylpiperazine (2.2 g, 22.1 mmol, 1.0 eq.), tris(dibenzylidene acetone)dipalladium(0) (607 mg, 0.66 mmol, 0.03 eq.) and (+/−)-BINAP (137 mg, 0.22 mmol; 0.01 eq.) in toluene was degassed 15 min under N2. 4-bromo-4′-fluorobiphenyl (4.99 g, 19.9 mmol, 0.90 eq.) was added followed by sodium tert-butoxide (2.97 g, 30.9 mmol, 1.4 eq.). The resulting mixture was heated to 90° C. for 14 h. The reaction was cooled to room temperature, filtered on a bed of cellite and washed with Et2O. The combined organic layers were then washed with H2O (3×), dried over MgSO4, filtered and evaporated to give a dark brown oil. This residue was purified by chromatography on silicagel (DCM/MeOH 20/80) to give the title product as off white solid (3.0 g, 50%) M+(ESI): 271.3. HPLC (Condition A), Rt: 2.8 min (HPLC purity: 99.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08247437B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-e30c30f8202a4c03823de19e0edd85f3 |
|---|
| Source note | uspto-grants-2012_08 |
|---|