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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1270716Erstellt: 26. Oktober 2026

Potassium Carbonate → 2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)aniline

https://huagongshe.com/reaction/1270716

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktTriphenylphosphineHCID 11776—
Edukt4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
Edukt(3-Methoxyphenyl)boronic acidHCID 2734370—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)anilineHCID 18451489—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

2,3,5,6-Tetrafluoro-4-bromoaniline (7.5 g, 30.7 mmol) is dissolved in DME (150 mL) and treated with 3-methoxyphenylboronic acid (4.7 g, 30.7 mmol), a catalytic amount of tetrakistriphenylphosphine palladium(0) (0.70 g, 0.6 mmol) and triphenylphosphine (0.66 g, 2.5 mmol). Potassium carbonate (8.5 μg in 50 mL of water) is added and the reaction mixture stirred and 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-c0a8c1fe4a3c4fe9b0f239282dd887b2
Quellennotizuspto-grants-2007_04