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Hydroxyamine hydrochloride → HCID 76540720, 화합물

HRID 2060749
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HRID 2060749 반응식
[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]
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참가 물질

5

반응물 3

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

생성물 1

HCID 76540720HCID 76540720, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
70 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-83adc85bc82e4ca2ac37e0fc8bc1e496
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278441B2

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