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

HRID 1607753

反応式

HRID 1607753 の反応式
[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]

参加物

9

反応物 5

HCID 8929Sodium CyanideHCID 10420Acetonitrile, fluoro-HCID 25517Ammonium ChlorideHCID 1189271-Chloro-3-methoxypropaneHCID 5462224Magnesium

生成物 2

HCID 199663342-Amino-2-(fluoromethyl)-5-methoxypentanenitrile収率 99.9%HCID 178495109HCID 178495109、化合物

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-30 °C

実験手順

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 Perking, 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 mol) 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 (Na2SO 4), the combined organic extracts are evaporated to give 2-fluoromethyl-2-amino-5-methoxypentanenitrile (4.0 g) as a brown oil.

後処理

  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 (Na2SO 4)
  11. customthe combined organic extracts are evaporated

出典と根拠

ORDレコード
ord-90131712d2604b749ec11003cd0f12e7
出典データセット
uspto-grants-1989_09
特許番号
US04866206

関連ノート

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