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

HRID 1252563

Reaktionsgleichung

Reaktionsgleichung von HRID 1252563
[CH3:1][O:2][CH2:3][CH2:4][CH2:5]Cl.[Mg:7].[F:8][CH2:9][C:10]#[N:11].[C-:12]#[N:13].[Na+].[Cl-:15].[NH4+]>C1COCC1.O>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][Mg:7][Cl:15].[F:8][CH2:9][C:10]([NH2:11])([CH2:5][CH2:4][CH2:3][O:2][CH3:1])[C:12]#[N:13]

Komponenten

9

Reaktionsbedingungen

Temperatur
-30 °C

Versuchsvorschrift

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 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 (Na2SO4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.

Aufarbeitung

  1. customprepared
  2. temperatureThe mixture is heated
  3. temperatureunder reflux for 3 hours
  4. customat -30° C.
  5. customfor 1/2 hour
  6. additionis added
  7. concentrationAfter saturating with sodium chloride
  8. customthe THF layer is separated
  9. extractionthe aqueous phase is extracted twice with ether
  10. dry with materialAfter drying (Na2SO4)
  11. customthe combined organic extracts are evaporated

Quellen und Nachweise

ORD-Eintrag
ord-2b7703a477ff49669e7de67f7572a85c
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04743691

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