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Hydroxyamine hydrochloride → 1-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone oxime

HRID 2071020
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HRID 2071020 반응식
[CH2:1]=[C:2]([C:4]1[CH:5]=[C:6]([C:10](=O)[CH3:11])[CH:7]=[N:8][CH:9]=1)[CH3:3].[NH2:13][OH:14].Cl>CCO.O.[OH-].[Na+]>[CH2:1]=[C:2]([C:4]1[CH:5]=[C:6]([C:10](=[N:13][OH:14])[CH3:11])[CH:7]=[N:8][CH:9]=1)[CH3:3]
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참가 물질

6

반응물 2

HCID 443297Hydroxyamine hydrochlorideHCID 686706051-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone

생성물 1

HCID 866474221-(5-(Prop-1-en-2-yl)pyridin-3-yl)ethanone oxime수율 79.4%

시약·촉매·용매 3

HCID 702Ethanol용매HCID 962Water용매HCID 14798Sodium Hydroxide용매

실험 절차

To a stirred solution of 1-(5-(prop-1-en-2-yl)pyridin-3-yl)ethanone (460 mg, 2.86 mmol) in 95% EtOH was added a solution of NH2OH.HCl (1.19 g, 17.14 mmol) in a mixture of water (5.8 mL) and 10% NaOH (5.8 mL) and refluxed for 2.5 h. All solvent was removed. The residue was dissolved in CHCl3, washed with water, dried with Na2SO4 and concentrated under reduced pressure to yield 400 mg of crude 1-(5-(prop-1-en-2-yl)pyridin-3-yl)ethanone oxime.

후처리

  1. temperaturerefluxed for 2.5 h
  2. customAll solvent was removed
  3. dissolutionThe residue was dissolved in CHCl3
  4. washwashed with water
  5. dry with materialdried with Na2SO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e147ab0d50b442a9884cffd846ce1bdc
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299267B2

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