Sodium Cyanide → 5,5,5-Trifluoropentanenitrile

HRID 36204

反応式

HRID 36204 の反応式
[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]

参加物

4

反応条件

温度
80 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-4edbc26da4a8457da8b990ef58a7da39
出典データセット
uspto-grants-1995_05
特許番号
US05411980

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