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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1411413Erstellt: 24. Oktober 2026

Cesium carbonate → 4-Cyclopropyl-3,5-difluoroaniline

https://huagongshe.com/de/reaction/1411413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukt4-Bromo-3,5-difluoroanilineHCID 2736260—
EduktPotassiumHCID 5462222—
EduktCyclopropyltrifluoroborateHCID 16217981—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorPhosphine, butylbis(tricyclo(3.3.1.13,7)dec-1-yl)-, hydriodide (1:1)HCID 66629336—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt4-Cyclopropyl-3,5-difluoroanilineHCID 6663050682%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a pressure tube was added 4-bromo-3,5-difluoroaniline (1.0 g, 4.8 mmol), cesium carbonate (4.7 g, 14.4 mmol), toluene (10 mL) and water (1 mL). The solution was de-gassed with N2 gas for 30 minutes, followed by the addition of cyclopropyltrifluoro-borate, potassium salt (0.8 g, 5.3 mmol), di(1-adamantyl)-n-butylphosphine hydroiodide (0.07 g, 0.14 mmol) and palladium(II) acetate (0.02 g, 0.096 mmol). De-gassing was continued for 5 minutes, the tube was sealed and heated at 100° C. for 18 hours. The cooled solution was diluted with EtOAc, washed with H2O and brine, dried (Na2SO4), and filtered. The filtrate was treated with 3-mercaptopropyl silica gel for 1 hour. The mixture was filtered and concentrated to give crude product which was purified by flash chromatography (0-30% EtOAc/hexane) to give the title compound (0.67 g, 4.0 mmol, 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08921514B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-9e4d9da843e449fe9bdd8ae3aa784ffa
Quellennotizuspto-grants-2014_12