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

HRID 1105615

Reaktionsgleichung

Reaktionsgleichung von HRID 1105615
[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 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.

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-791213980e6741aea291d0ca425a56ec
Quelldatensatz
uspto-grants-1982_01
Patentnummer
US04309442

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