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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341363Erstellt: 27. Oktober 2026

Aniline → 3,5-Difluoro-n-phenylaniline

https://huagongshe.com/reaction/341363

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktPotassium HydroxideHCID 14797—
Edukt1,3-Difluoro-5-iodobenzeneHCID 2778221—
KatalysatorHexadecyltrimethylammonium BromideHCID 5974—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelSodium chloride; waterHCID 57417360—
Produkt3,5-Difluoro-n-phenylanilineHCID 24225420,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

In a 5 mL microwave reaction vial was placed aniline (0.298 g. 3.20 mmol) and 1,3-difluoro-5-iodobenzene (0.768 g, 3.20 mmol) in toluene (3 mL). KOH (0.323 g, 5.76 mmol) in water (650 μL) and N,N,N-trimethylhexadecan-1-aminium bromide (6.30 mg, 0.017 mmol) were added to the vial with stirring. After the reaction was warmed to 90° C., bis[tri(t-butylphosphine]palladium[0] (0.016 g, 0.032 mmol) was added and the reaction was stirred at 150° C. for 4 h and then 160° C. for 2 h. The mixture was diluted with water and brine, and extracted with toluene. The toluene extract was subsequently washed with water, dried over MgSO4 and concentrated. The residue was purified by flash column chromatography to provide the title compound as a brown oil (0.132 g). LCMS m/z=206.2 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 6.54 (tt, J=9.35, 2.27 Hz, 1H), 6.63 (dd, J=10.48, 2.15 Hz, 2H), 7.01 (dt, J=14.65, 1.14 Hz, 1H), 7.17 (dd, J=8.59, 1.01 Hz, 2H), 7.34 (t, J=7.83 Hz, 2H), 8.69 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895776B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-608f679dbbd647098ca57e81b68c3f0e
Quellennotizuspto-grants-2014_11