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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktTri-o-tolylphosphineHCID 80271—
Edukt4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
Edukt(3-Methoxyphenyl)boronic acidHCID 2734370—
Katalysatorpalladium(II) acetateHCID 167845—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)anilineHCID 18451489—

Reaktionsbedingungen

Temperatur90 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07202364B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-2811fa6bb2e04daaa00cb5e2387f1aa1
Quellennotizuspto-grants-2007_04