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Hydrogen Peroxide → alpha-(2,4-difluorophenyl)-N-[dimethyl(methoxymethyl) methyl]nitrone

HRID 636735
ノート
印刷プレビュー

反応式

HRID 636735 の反応式
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][NH:10][C:11]([CH3:16])([CH3:15])[CH2:12][O:13][CH3:14].[OH:17]O.[Na+].[Cl-]>CO>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH:9]=[N+:10]([C:11]([CH3:16])([CH3:15])[CH2:12][O:13][CH3:14])[O-:17]
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 5234Sodium ChlorideHCID 21255704N-(2,4-difluorophenylmethyl)-N-[dimethyl(methoxymethyl)methyl]amine

生成物 1

HCID 72602289alpha-(2,4-difluorophenyl)-N-[dimethyl(methoxymethyl) methyl]nitrone収率 51%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of N-(2,4-difluorophenylmethyl)-N-[dimethyl(methoxymethyl)methyl]amine obtained in Example 14 (378.8 mg, 1.65 mmol) and Na2WO4 2H2O (84.3 mg, 0.256 mmol) in methanol (5 ml) was cooled to 0° C. in ice-water bath. To the mixture was added dropwise 31% H2O2 aqueous solution (439.3 mg, 4.00 mmol). After addition the mixture was gradually warmed to room temperature and stirred for 15 hours. The mixture was added to sat. NaCl aqueous solution and extracted three times with ethyl acetate and dried over MgSO4. The mixture was concentrated and purified by silica gel chromatography (toluene/ethyl acetate=5/1) to give the title compound (204.8 mg; 51%).

後処理

  1. additionAfter addition the mixture
  2. extractionextracted three times with ethyl acetate
  3. dry with materialdried over MgSO4
  4. concentrationThe mixture was concentrated
  5. custompurified by silica gel chromatography (toluene/ethyl acetate=5/1)

出典と根拠

ORDレコード
ord-4d225aabeb784a0ca64a287642cac08b
出典データセット
uspto-grants-2001_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06194461B1

反応ノート

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