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Hydrogen Peroxide → HCID 20725604、化合物

HRID 2190859
ノート
印刷プレビュー

反応式

HRID 2190859 の反応式
[CH3:1][O:2][CH2:3][C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1.OO.C(=O)([O-])[O-:13].[Na+].[Na+]>C(O)(=O)C>[CH3:1][O:2][CH2:3][C:4]1[CH:5]=[N+:6]([O-:13])[CH:7]=[CH:8][CH:9]=1
参加物反応条件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 10340Sodium CarbonateHCID 3389263-(Methoxymethyl)pyridine

生成物 1

HCID 20725604HCID 20725604、化合物

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
80 °C

実験手順

A mixture of 7.74 g of 3-methoxymethylpyridine, 60 ml of acetic acid and 7.5 g of 30% hydrogen peroxide solution was stirred while heating at 80° C. for four hours. The reaction mixture was cooled to room temperature, and then sodium carbonate was added in small portions. The reaction mixture was subjected to filtration, and washed with ethyl acetate. The resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite and a saturated sodium chloride solution, and dried over anhydrous sodium carbonate. Activated carbon was added, followed by filtration through Celite™. The filtrate was concentrated under reduced pressure to give 2.66 g of 3-methoxymethylpyridine N-oxide.

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationThe reaction mixture was subjected to filtration
  3. washwashed with ethyl acetate
  4. washThe resultant filtrate was washed with a saturated aqueous solution of sodium hydrogensulfite
  5. dry with materiala saturated sodium chloride solution, and dried over anhydrous sodium carbonate
  6. additionActivated carbon was added
  7. filtrationfollowed by filtration through Celite™
  8. concentrationThe filtrate was concentrated under reduced pressure

出典と根拠

ORDレコード
ord-e58c21cc6e384f8a88263d6c280fd794
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324387B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート