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
- concentrationThe solution was concentrated in vacuo
- dissolutionthe residue was dissolved in EtOAc
- stirringstirred at RT
- filtrationThe solid was filtered
- customthe filtrate was evaporated
- customto obtain the crude product
- 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
関連ノート
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