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Hydroxyamine hydrochloride → HCID 76540720、化合物

HRID 2060749
ノート
印刷プレビュー

反応式

HRID 2060749 の反応式
[CH2:1]([O:4][CH2:5][C:6]([C:8]1[CH:13]=[C:12]([Br:14])[CH:11]=[CH:10][C:9]=1[F:15])=O)[CH:2]=[CH2:3].Cl.[NH2:17][OH:18].C([O-])(=O)C.[Na+]>C(O)C>[CH2:1]([O:4][CH2:5][C:6]([C:8]1[CH:13]=[C:12]([Br:14])[CH:11]=[CH:10][C:9]=1[F:15])=[N:17][OH:18])[CH:2]=[CH2:3]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 443297Hydroxyamine hydrochlorideHCID 517045Sodium AcetateHCID 574757622-(Allyloxy)-1-(5-bromo-2-fluorophenyl)ethanone

生成物 1

HCID 76540720HCID 76540720、化合物

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
70 °C

実験手順

To a solution of 2-(allyloxy)-1-(5-bromo-2-fluorophenyl)ethanone (118 g, 432.1 mmol) in ethanol (1.7 L) is added hydroxylamine hydrochloride (34.5 g, 496.9 mmol) and sodium ethanoate (40.8 g, 496.9 mmol) at 25° C. The reaction is heated at 70° C. for 1 hr. The reaction is cooled and the solvent is removed under reduced pressure. The residue is washed with water (1 L) and is extracted three times with dichloromethane (3×500 mL). The organic phase is dried over magnesium sulfate, filtered, and the solvent is removed under reduced pressure, to obtain the title compound as a mixture of two possible oximes (120 g, 96%). ES/MS m/e (79Br/81Br) 288, 290 (M+1).

後処理

  1. temperatureThe reaction is cooled
  2. customthe solvent is removed under reduced pressure
  3. washThe residue is washed with water (1 L)
  4. extractionis extracted three times with dichloromethane (3×500 mL)
  5. dry with materialThe organic phase is dried over magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent is removed under reduced pressure

出典と根拠

ORDレコード
ord-83adc85bc82e4ca2ac37e0fc8bc1e496
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08278441B2

反応ノート

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