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Sulfolane → 2-Fluoro-5-nitropyridine

HRID 395913
ノート
印刷プレビュー

反応式

HRID 395913 の反応式
[N+:1]([C:4]1[CH:5]=[CH:6][C:7](Cl)=[N:8][CH:9]=1)([O-:3])=[O:2].[F-:11].[K+].C1CS(=O)(=O)CC1>C1C=CC=CC=1>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([F:11])=[N:8][CH:9]=1)([O-:3])=[O:2]
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 31347SulfolaneHCID 783082-Chloro-5-nitropyridineHCID 522689Potassium Fluoride

生成物 1

HCID 952642-Fluoro-5-nitropyridine

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

A mixture of 5-nitro-2-chloropyridine (2.0 g, 12.6 mmol) and anhydrous potassium fluoride (2.2 g, 38 mmol) in a combination of sulfalone (6 mL) and benzene (4 mL) was stirred at RT for 20 min. The benzene was then removed by distillation. The resulting mixture was heated at 150° C. for 12 h. The mixture was cooled to RT whereupon water (60 mL) was added. The desired product was separated from the solution via steam distillation. Extraction of the distillate with diethyl ether (2×10 mL) followed by drying (Na2SO4) and concentration gave 5-nitro-2-fluoropyridine as a water white oil (1.3 g, 73%).

後処理

  1. customThe benzene was then removed by distillation
  2. temperatureThe resulting mixture was heated at 150° C. for 12 h
  3. temperatureThe mixture was cooled to RT whereupon water (60 mL)
  4. additionwas added
  5. customThe desired product was separated from the solution via steam distillation
  6. extractionExtraction of the distillate with diethyl ether (2×10 mL)
  7. customby drying
  8. concentration(Na2SO4) and concentration

出典と根拠

ORDレコード
ord-949b3abdd77d4b8396530941a4ae092d
出典データセット
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06605725B2

反応ノート

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