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N-(2-Methoxyethyl)-2-nitroaniline → 1-N-(2-methoxyethyl)benzene-1,2-diamine

HRID 1096655
ノート
印刷プレビュー

反応式

HRID 1096655 の反応式
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-])=O>CO.C(O)(=O)C.[Zn]>[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[C:7]([NH2:12])=[CH:8][CH:9]=[CH:10][CH:11]=1
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 1

HCID 10375425N-(2-Methoxyethyl)-2-nitroaniline

生成物 1

HCID 102614521-N-(2-methoxyethyl)benzene-1,2-diamine収率 72%

試薬・触媒・溶媒 3

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒HCID 887Methanol溶媒

実験手順

The residue 109A was dissolved in methanol (60 mL) and acetic acid (4 mL). Zinc metal (3.24 g, 49.6 mmol) was added and the mixture was stirred overnight at room temperature. The reaction was decanted off from unreacted zinc metal. The solvent was removed under vacuum and resuspended in ethyl acetate (30 mL). The precipitate was removed by filtration on a Buchner funnel with Celite. Solvent was removed from the filtrate and the residue was purified by column chromatography (2% MeOH/DCM) to give the product N1-(2-methoxyethyl)benzene-1,2-diamine (109B) as a red oil (422 mg, 72% yield over two steps). ESI-MS:m/z 167.4 (M+H)+.

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

後処理

  1. customThe reaction was decanted off from unreacted zinc metal
  2. customThe solvent was removed under vacuum
  3. customThe precipitate was removed by filtration on a Buchner funnel with Celite
  4. customSolvent was removed from the filtrate
  5. customthe residue was purified by column chromatography (2% MeOH/DCM)

出典と根拠

ORDレコード
ord-46108410ddf843bca44d8d93e7125b22
出典データセット
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08138168B1

反応ノート

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