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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602676Erstellt: 25. Oktober 2026

Triethylamine → Methyl {1-[1-(4-chlorophenyl)ethyl]azetidin-3-yl}(3,5-difluorophenyl)acetate

https://huagongshe.com/reaction/602676

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4'-ChlorovalerophenoneHCID 90686—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktMethyl azetidin-3-yl(3,5-difluorophenyl)acetateHCID 67065947—
Lösungsmittel1,1-DichloroethaneHCID 6365—
ProduktMethyl {1-[1-(4-chlorophenyl)ethyl]azetidin-3-yl}(3,5-difluorophenyl)acetateHCID 86609768—

Reaktionsschritte

A solution of 0.015 g (0.054 mmole) of methyl azetidin-3-yl(3,5-difluorophenyl)acetate, 0.020 g (0.101 mmol) of 1-(4-chlorophenyl)pentan-1-one and 0.015 mL (0.12 mmol) of triethylamine in 5 mL of dichloroethane was stirred at room temperature. After 5 min, 0.050 g (0.237 mmol) of sodium triacetoxyborohydride was added and the mixture was stirred at room temperature for 6 h. The reaction was quenched by addition of saturated K2CO3 solution and the mixture was partitioned between 10 mL ether and 2 mL saturated K2CO3 solution. The layers were separated and the organic layer was dried over Na2SO4, and concentrated. The residue was purified by reverse phase chromatography (Waters Xterra C18, 19 mm×10 mm) using a gradient of CH3CN—H2O-Et3N (20:80:0.1 to 60:40:0.1). Homogenous fractions were pooled and concentrated to afford the title compound as a mixture of isomers; Mass Spectrum: m/e=422 (M+1 35Cl and 424 (M+1 37Cl). Mass Spectrum: m/e=422 (M+1 35Cl and 424 (M+1 37Cl).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07906503B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-8a04fb2f3333474f9374b64141d63907
Quellennotizuspto-grants-2011_03