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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1638157Erstellt: 27. Oktober 2026

Bromoacetonitrile → beta-(R)-(2-fluorophenyl)-gamma,2-dioxo-4(R)-phenyl-3-oxazolidinebutyronitrile

https://huagongshe.com/reaction/1638157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromoacetonitrileHCID 11534—
EduktAmmonium ChlorideHCID 25517—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinoneHCID 11150697—
LösungsmittelTetrahydrofuranHCID 8028—
Produktbeta-(R)-(2-fluorophenyl)-gamma,2-dioxo-4(R)-phenyl-3-oxazolidinebutyronitrileHCID 11089040—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

To a solution of 3-[(2-fluorophenyl)-acetyl]-4(R)-phenyl-2-oxazolidinone (435 g, 1.45 mol) in THF (6000 mL), is added sodium hexamethyldisilazide [(TMS)2NNa, 1M in THF, 1480 ml, 1.48 mol] dropwise at -78° C. The resulting mixture is then warmed to -30° C. and stirred for 2.5 hours. After this time the reaction mixture is recooled to -78° C. and a solution of BrCH2CN (175 g, 1.46 mmol) in THF (200 mL) is added. The reaction mixture is then warmed to -40° C. and stirred for 2 hours. Subsequently the resulting solution is treated with saturated NH4Cl (1×3000 ml) and extracted with EtOAc (1×3000 mL). The organic layer is separated, washed with H2O (1×1500 mL), saturated NaCl solution (2×1500 mL), dried over MgSO4 and concentrated in vacuo, to provide 3-[(R)-β-cyano-α-(2-fluorophenyl)-propionyl]-4-(R)-phenyl-2-oxazolidinone, m.p. 179-181° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06043365
Quelldatensatzuspto-grants-2000_03
ORD IDord-724b76e8e1424ee0b27432583bbfea09
Quellennotizuspto-grants-2000_03