HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1270717Erstellt: 26. Oktober 2026
Potassium Carbonate → 2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)aniline
https://huagongshe.com/reaction/1270717
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Tri-o-tolylphosphine | HCID 80271 | — |
| Edukt | 4-Bromo-2,3,5,6-tetrafluoroaniline | HCID 618671 | — |
| Edukt | (3-Methoxyphenyl)boronic acid | HCID 2734370 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | 2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)aniline | HCID 18451489 | — |
Reaktionsschritte
Alternative procedure: 2,3,5,6-Tetrafluoro-4-bromoaniline (12.0 g, 49.2 mmol) is dissolved in DME (250 mL) and treated with 3-methoxyphenylboronic acid (7.5 g, 49.2 mmol), a catalytic amount of palladium(II) acetate (0.23 g, 1.0 mmol) and tri-o-tolylphosphine (1.22 g, 4.0 mmol). Potassium carbonate (13.6 g in 50 mL water) is added and the reaction mixture stirred, purged with nitrogen, then heated to 90° C. for 24 hours. After cooling to room temperature most of the DME is removed by rotary evaporator under high vacuum. The resulting material is partitioned between EtOAc (200 mL) and water (250 mL). The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator. The crude reaction product is purified by flash chromatography (9:1 hexanes/EtOAc, then 6:4 hexanes/EtOAc) to give 2,3,5,6-tetrafluoro-4-(3′-methoxyphenyl)aniline (m.p. 94–96° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07202364B2 |
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| Quelldatensatz | uspto-grants-2007_04 |
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| ORD ID | ord-2811fa6bb2e04daaa00cb5e2387f1aa1 |
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| Quellennotiz | uspto-grants-2007_04 |
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