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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 19791Erstellt: 24. Oktober 2026

Potassium Phosphate, Tribasic → 3-Cyclopropyl-4-fluoroaniline

https://huagongshe.com/de/reaction/19791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
EduktTricyclohexylphosphineHCID 75806—
EduktCyclopropylboronic acidHCID 2760897—
Edukt3-Bromo-4-fluoroanilineHCID 2779286—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
Produkt3-Cyclopropyl-4-fluoroanilineHCID 5741630364%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 3-bromo-4-fluorophenylamine (synthesized as described in J. Org. Chem. 1981, 46, 2280-2286) (415 mg, 2.18 mmol), cyclopropyl boronic acid (244 mg, 2.84 mmol), potassium phosphate (1.62 g, 7.64 mmol), and tricyclohexyl phosphine (61 mg, 0.22 mmol) in toluene (10 ml) and water (0.5 ml) was added palladium acetate (25 mg, 0.11 mmol) and the reaction mixture was heated to 100° C. overnight. The mixture was then cooled to RT and diluted with water and extracted with ether. The organic phases were combined, washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography to give 3-cyclopropyl-4-fluorophenylamine (210 mg, 64%). MS (ISP) 152.2 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745477B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-14b57bd0666e45aab253ce6c60b843fa
Quellennotizuspto-grants-2010_06