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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72402Erstellt: 24. Oktober 2026

Acetonitrile → 1-benzhydryl-N-(4-fluorophenyl)azetidin-3-amine

https://huagongshe.com/de/reaction/72402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt4-FluoroanilineHCID 9731—
Edukt1-(Diphenylmethyl)azetidin-3-yl methanesulfonateHCID 2758716—
Produkt1-benzhydryl-N-(4-fluorophenyl)azetidin-3-amineHCID 67958229—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 4-fluoro aniline (0.412 ml, 4.296 mmol) in acetonitrile (10 ml) potassium carbonate (771 mg, 5.584 mmol) was added followed by addition of 1-benzhydrylazetidin-3-yl methanesulfonate (D19) (1.5 g, 4.72 mmol). The reaction mixture was stirred at 100° C. for 5 minutes under microwave irradiation. Solvents were evaporated under vacuo and the residue was taken in with diethylether (50 ml) then water (50 ml) was added. The aqueous layer was extracted with diethylether (2×30 ml). The organics after solvent evaporation were purified by Biotage SNAP-Si cartridge (25 g) eluting with cyclohexane/ethylacetate from 100-0 to 85/15. Collected fractions, after solvent evaporation afforded the title (D24) (0.5 g)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828987B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d2e0bd68ea8f4e4da0edbf7e1c4971e9
Quellennotizuspto-grants-2014_09