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2,5-Difluorobenzaldehyde → 1-(2,5-Difluorophenyl)ethan-1-one

HRID 3684
ノート
印刷プレビュー

反応式

HRID 3684 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[CH:4]=[O:5].[CH3:11]Br.[Mg]>O1CCCC1>[F:1][C:2]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[C:4](=[O:5])[CH3:11]
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 1376632,5-DifluorobenzaldehydeHCID 86584079Magnesium methylbromide

生成物 1

HCID 747941-(2,5-Difluorophenyl)ethan-1-one収率 84%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution (100 ml) of 2,5-difluorobenzaldehyde (24.6 g) in tetrahydrofuran was dropwise added to an ice-cooled solution (207 ml) of 0.92N magnesium methylbromide in tetrahydrofuran. The resulting solution was stirred at room temperature for 1.5 hours, and the organic phase was washed in a saturated sodium chloride solution and dried over anhydrous magnesium sulfate, to subsequently distill off the solvents under reduced pressure. To the residue were added anhydrous dichloromethane (500 ml), sodium acetate (14.2 g) and pyridinium chlorochromate (55.94 g), prior to stirring at room temperature for 10 hours. To the resulting mixture was added an aqueous saturated sodium hydrogen carbonate solution, prior to extraction in ethyl acetate three times. The organic phase was washed in water and in a saturated sodium chloride solution and dried over anhydrous magnesium sulfate, to distill off the solvents under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=85:15), to recover 2',5'-difluoroacetophenone (22.73 g; yield of 84%). By 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

後処理

  1. washthe organic phase was washed in a saturated sodium chloride solution
  2. dry with materialdried over anhydrous magnesium sulfate
  3. distillationto subsequently distill off the solvents under reduced pressure
  4. additionTo the residue were added anhydrous dichloromethane (500 ml), sodium acetate (14.2 g) and pyridinium chlorochromate (55.94 g)
  5. stirringto stirring at room temperature for 10 hours
  6. additionTo the resulting mixture was added an aqueous saturated sodium hydrogen carbonate solution
  7. extractionto extraction in ethyl acetate three times
  8. washThe organic phase was washed in water and in a saturated sodium chloride solution
  9. dry with materialdried over anhydrous magnesium sulfate
  10. distillationto distill off the solvents under reduced pressure
  11. customThe residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=85:15)

出典と根拠

ORDレコード
ord-fd7bd30d38484bb09e3a0ae03fe39a9e
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05734067

反応ノート

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