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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1105615Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1105615

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 19966334—
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 Perkin, 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 ml) 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 hours at room temperature. After saturating with sodium chloride, the THF layer is separated and the aqueous phase is extracted twice with ether. After drying (Na2SO4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxyvaleronitrile (4.0 g) as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04309442
Quelldatensatzuspto-grants-1982_01
ORD IDord-791213980e6741aea291d0ca425a56ec
Quellennotizuspto-grants-1982_01