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

HRID 1065677

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HRID 1065677 반응식
[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]

참가 물질

9

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온도
-30 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-63f2d3c1f3a04870a6a268b8fcf77aca
출처 데이터셋
uspto-grants-1982_05
특허 번호
US04330559

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