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2,5-Dichlorophenol → 2,5-Dichloro-4-nitrophenol

HRID 1957470
ノート
印刷プレビュー

反応式

HRID 1957470 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[CH:4][C:3]=1[OH:9].[N+:10]([O-])([OH:12])=[O:11]>ClCCl>[Cl:1][C:2]1[CH:7]=[C:6]([N+:10]([O-:12])=[O:11])[C:5]([Cl:8])=[CH:4][C:3]=1[OH:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 662,5-DichlorophenolHCID 944Nitric Acid

生成物 1

HCID 221082,5-Dichloro-4-nitrophenol収率 31%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

2,5-dichlorophenol (72 g, 440 mmol) were slurried in 100 ml dichloromethane which resulted in an endothermic reaction. To this mixture were slowly added 30 ml (480 mmol) concentrated nitric acid. The reaction was allowed to reach and maintain reflux. The mixture was stirred until it reached ambient temperature and all materials remained in solution. 50 g of ice were added and solids precipitated. The mixture was filtered cold and washed with 25 ml dichloromethane, 50 ml dichloromethane, then twice with 25 ml dichloromethane to yield 28.4 g of 2,5-dichloro-4-nitrophenol.

後処理

  1. customresulted in an endothermic reaction
  2. temperaturemaintain
  3. temperaturereflux
  4. customreached ambient temperature
  5. customsolids precipitated
  6. filtrationThe mixture was filtered cold
  7. washwashed with 25 ml dichloromethane, 50 ml dichloromethane

出典と根拠

ORDレコード
ord-dac27d0877c748b2bf7ed384d762bcf7
出典データセット
uspto-grants-1998_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05786301

反応ノート

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