Hydroxyamine hydrochloride → 4,4,4-trifluoro-N'-hydroxy-3-methoxybut-2-enimidamide

HRID 631543ノート

反応式

HRID 631543 の反応式
Cl.[NH2:2][OH:3].C[O-].[Na+].[F:7][C:8]([F:16])([F:15])[C:9]([O:13][CH3:14])=[CH:10][C:11]#[N:12]>CO>[F:7][C:8]([F:16])([F:15])[C:9]([O:13][CH3:14])=[CH:10][C:11](=[N:2][OH:3])[NH2:12]

参加物

5

反応条件

温度
0 °C

実験手順

Hydroxylamine hydrochloride (2.88 g, 41. 5 mmol) was dissolved in methanol (20 mL) and cooled to 0° C. in an ice-bath. Sodium methoxide (2.24 g, 41.5 mmol) was added and the resulting suspension stirred at room temperature for 15 minutes. The suspension was cooled to 0° C., 4,4,4-trifluoro-3-methoxybut-2-enenitrile (26 mmol) was added dropwise and the mixture allowed to slowly warm to room temperature. The mixture was then heated to 60° C. overnight. The white solid was removed by filtration, washed with dichloromethane and the filtrate concentrated under reduced pressure to afford 4,4,4-trifluoro-N′-hydroxy-3-methoxybut-2-enimidamide as a solid, which was used directly in the next step without further purification. The solid was taken in ethanol (25 mL) and the solution acidified (pH=1) with 37% aqueous hydrochloric acid. The resulting mixture was heated to 60° C. for 2h. Ethanol was removed under reduced pressure and the residue diluted with dichloromethane. A saturated solution of sodium bicarbonate was added (pH=14) and the organic phase separated. The aqueous phase was back extracted three times with dichloromethane, the organics combined, dried (MgSO4) and concentrated under reduced pressure. The resulting crude material was purified by silica gel chromatography (dichloromethane/ethyl acetate 95:5) to isolate 3-(trifluoromethyl)isoxazol-5-amine (446 mg, 11%) along with 5-(trifluoromethyl)isoxazol-3-amine as a minor product. 1H NMR (300 MHz, CDCl3) δ 5.31 (s, 1H), 5.03 (bs, 2H).

後処理

  1. temperatureThe suspension was cooled to 0° C.
  2. temperatureto slowly warm to room temperature
  3. temperatureThe mixture was then heated to 60° C. overnight
  4. customThe white solid was removed by filtration
  5. washwashed with dichloromethane
  6. concentrationthe filtrate concentrated under reduced pressure

出典と根拠

ORDレコード
ord-8014a4bc356d4ead850d951a6aac2edf
出典データセット
uspto-grants-2016_04
特許番号
US09320739B2

反応ノート

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