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Hydroxylamine HCl → Methyl 2-((5-(1-(hydroxyimino)ethyl)pyridin-2-yl)oxy)acetate

HRID 68310
ノート
印刷プレビュー

反応式

HRID 68310 の反応式
[C:1]([C:4]1[CH:5]=[CH:6][C:7]([O:10][CH2:11][C:12]([O:14][CH3:15])=[O:13])=[N:8][CH:9]=1)(=O)[CH3:2].C([O-])(=O)C.[Na+].[Cl-].[OH:22][NH3+:23]>C(O)C.O>[OH:22][N:23]=[C:1]([C:4]1[CH:5]=[CH:6][C:7]([O:10][CH2:11][C:12]([O:14][CH3:15])=[O:13])=[N:8][CH:9]=1)[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 21645Hydroxylamine HClHCID 517045Sodium AcetateHCID 68281905Methyl 2-((5-acetylpyridin-2-yl)oxy)acetate

生成物 1

HCID 86699620Methyl 2-((5-(1-(hydroxyimino)ethyl)pyridin-2-yl)oxy)acetate収率 88%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water
溶媒

実験手順

To a solution of methyl 2-((5-acetylpyridin-2-yl)oxy)acetate (1.23 gm, 0.059 mole) in ethanol (10 mL), a solution of sodium acetate (0.942 gm, 0.0117 mole) and hydroxylammonium chloride (1.2 gm, 0.0117 mole) in water (5 ml) was added and the reaction mixture was refluxed for 1 h. The reaction mixture was coiled to room temperature and solvent was evapourated in vacuum. The residue was diluted with ice cold water and solid seperated was filtered, washed with water and dried over P2O5 under vacuum to yield 1.15 gm (88%) of title product as off white solid.

後処理

  1. temperaturethe reaction mixture was refluxed for 1 h
  2. customwas coiled to room temperature
  3. additionThe residue was diluted with ice cold water and solid
  4. customseperated
  5. filtrationwas filtered
  6. washwashed with water
  7. dry with materialdried over P2O5 under vacuum

出典と根拠

ORDレコード
ord-c52054b585b049c482cb8432945af5a3
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08822414B2

反応ノート

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