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1-Chloro-4-nitrobenzene → p-Fluoronitrobenzene

HRID 9922
ノート
印刷プレビュー

反応式

HRID 9922 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7](Cl)=[CH:6][CH:5]=1)([O-:3])=[O:2].[F-:11].[K+]>CS(C)=O>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([F:11])=[CH:6][CH:5]=1)([O-:3])=[O:2]
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

4

反応物 2

HCID 74741-Chloro-4-nitrobenzeneHCID 522689Potassium Fluoride

生成物 1

HCID 9590p-Fluoronitrobenzene収率 96%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
170 °C

実験手順

157 g of 4-nitrochlorobenzene, 200 g of dimethylsulfoxide, 62.7 g of potassium fluoride, and 2.49 g of (N,N-dimethylimidazolidino)tetramethyl-guanidinium chloride were placed in a 1 liter four-neck flask equipped with thermometer, anchor stirrer, and reflux condenser with bubble counter. The mixture was heated with stirring to 170° C. and kept at this temperature for 5 hours. The reaction mixture was then cooled to room temperature, water was added at a volumetric ratio of 1:1, the phases that formed were separated, and, from the organic phase, by fractional distillation at reduced pressure, 4-nitrofluorobenzene was obtained in a yield of 96% of theory.

後処理

  1. customequipped with thermometer, anchor stirrer
  2. temperaturereflux condenser
  3. customwith bubble counter
  4. temperatureThe mixture was heated
  5. temperatureThe reaction mixture was then cooled to room temperature
  6. additionwater was added at a volumetric ratio of 1:1
  7. customthe phases that formed
  8. customwere separated
  9. distillationfrom the organic phase, by fractional distillation at reduced pressure

出典と根拠

ORDレコード
ord-9a8619cf766f4e9b8699861270e51844
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07091362B2

反応ノート

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