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Hydrogen Peroxide → HCID 11819636、化合物

HRID 1491829
ノート
印刷プレビュー

反応式

HRID 1491829 の反応式
OO.[C:3]([NH:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1)(=[O:5])[CH3:4].S([O-])([O-])=[O:16].[Na+].[Na+]>C(O)(=O)C>[C:3]([NH:6][CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N+:10]=1[O-:16])(=[O:5])[CH3:4]
参加物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 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 238301N-(2-(Pyridin-2-yl)ethyl)acetamide

生成物 1

HCID 11819636HCID 11819636、化合物収率 100%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

30 wt % Hydrogen peroxide (80.3 ml) was added dropwise to a solution of 2-(2-acetylaminoethyl)pyridine (64.5 g) in acetic acid (65 ml) at 70°-75° C. and the mixture was stirred at the same temperature for 8 hours. After the mixture was ice-cooled and the mixture was added to a mixture of sodium sulfite (56.9 g) in ice water (200 ml). The solvent was removed by concentration in vacuo and the residue was extracted with a tetrahydrofuran. The extract solution was dried over magnesium sulfate and evaporated to give 2-(2-acetylaminoethyl)pyridine N-oxide (70.82 g).

後処理

  1. temperaturecooled
  2. customThe solvent was removed by concentration in vacuo
  3. extractionthe residue was extracted with a tetrahydrofuran
  4. dry with materialThe extract solution was dried over magnesium sulfate
  5. customevaporated

出典と根拠

ORDレコード
ord-691489eef06f4391a092e1a41c2e48a9
出典データセット
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05371097

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート