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HRID 1607753Erstellt: 25. Oktober 2026

Sodium Cyanide → 2-Amino-2-(fluoromethyl)-5-methoxypentanenitrile

https://huagongshe.com/reaction/1607753

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CyanideHCID 8929—
EduktAcetonitrile, fluoro-HCID 10420—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Chloro-3-methoxypropaneHCID 118927—
EduktMagnesiumHCID 5462224—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Amino-2-(fluoromethyl)-5-methoxypentanenitrileHCID 1996633499,9%
ProduktHCID 178495109HCID 178495109—

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

Under an atmosphere of nitrogen, 3-methoxypropyl magnesium chloride is prepared from 3-methoxy-1-chloropropane (5.43 g, 50 mmol), prepared according to Haworth and Perking, Chem. Zentralblatt, II, 1271 (1912) and magnesium turnings (1.22 g, 50 mmol) in dry THF (50 ml). The mixture is heated under reflux for 3 hours, then cooled to -30° C. and a solution of fluoroacetonitrile (2.95 g, 50 mmol) in THF (30 mol) is added during 20 minutes. After keeping the mixture at -30° C. for 1/2 hour more, a solution of sodium cyanide (4.9 g, 100 mmol) and ammonium chloride (8.09 g, 150 mmol) in water (100 ml), previously cooled to 0° C., is added and the mixture is stirred for 3/4 hour at room temperature. After saturating with sodium chloride, the THF layer is separated and the aqueous phase is extracted twice with ether. After drying (Na2SO 4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04866206
Quelldatensatzuspto-grants-1989_09
ORD IDord-90131712d2604b749ec11003cd0f12e7
Quellennotizuspto-grants-1989_09