HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium Carbonate → 2,3,5,6-Tetrafluoro-[1,1'-biphenyl]-4-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Phenylboronic Acid | HCID 66827 | — |
| Edukt | 4-Bromo-2,3,5,6-tetrafluoroaniline | HCID 618671 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2,3,5,6-Tetrafluoro-[1,1'-biphenyl]-4-amine | HCID 18451490 | — |
Reaktionsschritte
2,3,5,6-Tetrafluoro-4-bromoaniline (13.8 g, 56.7 mmol) is dissolved in benzene (200 mL) and treated with 1.5 equivalents of phenylboronic acid (10.4 g, 85.1 mmol) and a catalytic amount of tetrakistriphenylphosphine palladium(0) (4.2 g, 3.6 mmol) as a solution in ethanol (30 mL). Sodium carbonate (60 mL of 2 M aqueous solution) is added and the reaction mixture stirred and heated to reflux temperature for 24 hours. After cooling to room temperature the mixture is partitioned between Et2O (500 mL) and water (250 mL). The organic layer is washed with brine, dried (MgSO4) and concentrated by rotary evaporator. The residual oil is purified by flash chromatography (9:1 hexanes/EtOAc) to give 2,3,5,6-tetrafluoro-4-phenylaniline as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07202364B2 |
| Quelldatensatz | uspto-grants-2007_04 |
| ORD ID | ord-efd0175ca527483b827db0d3a68e28bf |
| Quellennotiz | uspto-grants-2007_04 |