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Methyl iodide → 2-(Methylamino)-4-nitrophenol

HRID 1585098
ノート
印刷プレビュー

反応式

HRID 1585098 の反応式
C([N:3]([CH2:6]C)[CH2:4][CH3:5])C.NC1C=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[OH:18].CI>CO>[CH3:6][NH:3][C:4]1[CH:5]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[OH:18]
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 6328Methyl iodide2 回HCID 8471Triethylamine2 回HCID 36133892-Amino-4-Nitrophenol

生成物 1

HCID 212217592-(Methylamino)-4-nitrophenol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
40 °C

実験手順

Triethylamine (2 ml, 14.4 mmol) was added to a solution of 2-amino-4-nitrophenol (1) (1.54 g, 10 mmol) and methyl iodide (1 ml, 16 mmol) in methanol (10 ml). After 1 hour at 40° C., further methyl iodide (1 ml) and triethylamine (1 ml) were added and the mixture was stirred at 40° C. for a further 2 hours. The reaction mixture was concentrated to dryness in vacuo, the residue was added to aqueous 2N sodium acetate solution and the mixture was extracted with ethyl acetate. The organic phase was dried with sodium sulfate and chromatographed on silica gel (eluent dichloromethane/methanol 95/5). Yield 880 mg (52%).

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

後処理

  1. concentrationThe reaction mixture was concentrated to dryness in vacuo
  2. additionthe residue was added to aqueous 2N sodium acetate solution
  3. extractionthe mixture was extracted with ethyl acetate
  4. dry with materialThe organic phase was dried with sodium sulfate
  5. customchromatographed on silica gel (eluent dichloromethane/methanol 95/5)

出典と根拠

ORDレコード
ord-66aae1aa20a84164b9801f127695ea82
出典データセット
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05935995

反応ノート

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