Potassium Cyanide → 3-(Trifluoromethyl)-1,2-oxazol-5-amine

HRID 1098554

反応式

HRID 1098554 の反応式
[C-:1]#[N:2].[K+].Br[CH2:5][C:6](=[N:11][OH:12])[C:7]([F:10])([F:9])[F:8]>CO>[F:8][C:7]([F:10])([F:9])[C:6]1[CH:5]=[C:1]([NH2:2])[O:12][N:11]=1

参加物

4

実験手順

To a suspension of KCN (1.90 g, 29.1 mmol) in MeOH (35 mL) was added dropwise 3-bromo-1,1,1-trifluoropropan-2-one oxime (5.00 g, 24.3 mmol) in MeOH (72 mL) at RT. The reaction mixture was stirred at RT for 3 hours. The solution was concentrated in vacuo, the residue was dissolved in EtOAc and stirred at RT. The solid was filtered and the filtrate was evaporated to obtain the crude product. The crude product was purified by silica gel column chromatography EtOAc/hexanes) to obtain 3-(trifluoromethyl)isoxazol-5-amine (1.38 g, 37% yield). MS (ESI) m/z: 153.0 (M+H+).

後処理

  1. concentrationThe solution was concentrated in vacuo
  2. dissolutionthe residue was dissolved in EtOAc
  3. stirringstirred at RT
  4. filtrationThe solid was filtered
  5. customthe filtrate was evaporated
  6. customto obtain the crude product
  7. customThe crude product was purified by silica gel column chromatography EtOAc/hexanes)

出典と根拠

ORDレコード
ord-c9d261f8f78b4c91b263dc66774f5a14
出典データセット
uspto-grants-2012_03
特許番号
US08143293B2

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