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3-Acetylpyridine → 1-(3-Pyridinyl)ethanone oxime

HRID 1651749
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HRID 1651749 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7](=O)[CH3:8])[CH:2]=1.Cl.[NH2:11][OH:12].C(=O)(O)[O-].[Na+]>CO.O>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7](=[N:11][OH:12])[CH3:8])[CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 95893-AcetylpyridineHCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium Bicarbonate

생성물 1

HCID 222791-(3-Pyridinyl)ethanone oxime수율 99.2%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A mixture of 50 g (0.41 mol) of 1-(3-pyridinyl)ethanone and 29 g (0.42 mol) of hydroxylamine hydrochloride in 250 ml of methanol was heated under reflux for five hours. Upon cooling to room temperature, a white solid separated from the reaction mixture. This material was collected by filtration and the filtrate was concentrated to yield additional white solid. The combined solids were dissolved in water and the solution was made weakly basic by the addition of sodium bicarbonate solution while cooling. The white precipitate which formed was separated by filtration to yield 55.4 g of 1-(3-pyridinyl)ethanone oxime, mp 115° -117° C.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for five hours
  3. customa white solid separated from the reaction mixture
  4. filtrationThis material was collected by filtration
  5. concentrationthe filtrate was concentrated
  6. customto yield additional white solid
  7. temperaturewhile cooling
  8. customThe white precipitate which formed
  9. customwas separated by filtration

출처 및 근거

ORD 기록
ord-942628025a3d4a15bf5f94c119c492c1
출처 데이터셋
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04929734

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