Sodium Cyanide → 5,5,5-Trifluoropentanenitrile

HRID 36204

Reaktionsgleichung

Reaktionsgleichung von HRID 36204
[C-:1]#[N:2].[Na+].[F:4][C:5]([F:11])([F:10])[CH2:6][CH2:7][CH2:8]Br>CS(C)=O>[F:4][C:5]([F:11])([F:10])[CH2:6][CH2:7][CH2:8][C:1]#[N:2]

Komponenten

4

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 882 mg (18 mmole) of sodium cyanide and 9 mL of DMSO was heated in an oil bath at 80° C. for 10 minutes until most of the solid had dissolved. The mixture was then removed from the oil bath and treated with 2.87 g (15 mmole) of 4,4,4-trifluorobutyl bromide. The mixture was heated to 110° C. for about 30 minutes and then cooled to room temperature. The mixture was partitioned between H2O and ether, and the aqueous layer was extracted with an additonal 2 portions of ether. The combined organic fractions were washed successively with 2N HCl (twice), H2O (twice), and brine. The ether phase was dried over anhydrous Na2SO4, filtered, and concentrated to yield 1.99 g (97%) of the title compound as a colorless liquid, suitable for use without further purification; IR (neat) νCO 2260 cm-1.

Aufarbeitung

  1. dissolutionhad dissolved
  2. customThe mixture was then removed from the oil bath
  3. temperatureThe mixture was heated to 110° C. for about 30 minutes
  4. temperaturecooled to room temperature
  5. customThe mixture was partitioned between H2O and ether
  6. extractionthe aqueous layer was extracted with an additonal 2 portions of ether
  7. washThe combined organic fractions were washed successively with 2N HCl (twice), H2O (twice), and brine
  8. dry with materialThe ether phase was dried over anhydrous Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-4edbc26da4a8457da8b990ef58a7da39
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05411980

Verknüpfte Notizen

Wird geladen…