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Sulfuric Acid → 2-Chloro-5-Fluorobenzaldehyde

HRID 1700758
ノート
印刷プレビュー

反応式

HRID 1700758 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH3:9].S(=O)(=O)(O)[OH:11].[Cr](O)(O)(=O)=O>C(OC(=O)C)(=O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]=[O:11]
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 1118Sulfuric AcidHCID 24425Chromic AcidHCID 1184752-Chloro-5-fluorotoluene

生成物 1

HCID 27791842-Chloro-5-Fluorobenzaldehyde

試薬・触媒・溶媒 1

HCID 7918Acetic Anhydride溶媒2 回

実験手順

To a solution of 2-chloro-5-fluorotoluene (5.0 g) in acetic anhydride (40 ml) was added dropwise under ice-cooling concentrated sulfuric acid (40 ml), and then added dropwise a solution of anhydrous chromic acid (9.3 g) in acetic anhydride (40 ml) for 2 hours. The mixture was stirred at the same temperature for 1 hour, poured into ice-water and extracted with diethylether. The organic layer was washed with sodium carbonate solution, water and saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was dissolved in tetrahydrofuran (10 ml). To the mixture were added water (4 ml) and concentrated sulfuric acid (4 ml), and the mixture was stirred at 100° C. for 30 minutes and cooled. The reaction solution was extracted with ethyl acetate. The organic layer was washed with sodium carbonate solution, water and saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated to give the residue, which was subjected to silica gel column chromatography to give 2-chloro-5-fluorobenzaldehyde (1.6 g).

後処理

  1. extractionextracted with diethylether
  2. washThe organic layer was washed with sodium carbonate solution, water and saturated brine
  3. dry with materialdried with magnesium sulfate
  4. customUnder reduced pressure, the solvent was evaporated
  5. dissolutionthe residue was dissolved in tetrahydrofuran (10 ml)
  6. additionTo the mixture were added water (4 ml) and concentrated sulfuric acid (4 ml)
  7. stirringthe mixture was stirred at 100° C. for 30 minutes
  8. temperaturecooled
  9. extractionThe reaction solution was extracted with ethyl acetate
  10. washThe organic layer was washed with sodium carbonate solution, water and saturated brine
  11. dry with materialdried with magnesium sulfate
  12. customUnder reduced pressure, the solvent was evaporated
  13. customto give the residue, which

出典と根拠

ORDレコード
ord-3dc7d39afae048f1b85e407f8da4d3f9
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06350749B1

反応ノート

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