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Benzene → 1-Phenyl-1,4-pentanedione

HRID 638799
ノート
印刷プレビュー

反応式

HRID 638799 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[O:5]=[C:6]([CH3:12])[CH2:7][CH2:8][C:9](Cl)=[O:10].Cl.[CH:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>>[C:14]1([C:9](=[O:10])[CH2:8][CH2:7][C:6](=[O:5])[CH3:12])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
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 4

HCID 241BenzeneHCID 313Hydrochloric AcidHCID 6451240Aluminum(III) ChlorideHCID 123004064-Oxopentanoyl chloride

生成物 1

HCID 1363711-Phenyl-1,4-pentanedione収率 24.07%

実験手順

To a well stirred suspension of anhydrous aluminium chloride (27.0 g, 205.9 mmol) in 126 ml of benzene was added 4-oxopentanoylchloride (23.0 g, 171.6 mmol) drop-wise, over a period of 30-35 minutes at room temperature (25-30° C.). The reaction mixture was stirred at the same temperature for 1 hour. After decomposition of the reaction mixture by the addition of solid ice and hydrochloric acid (10 ml) the precipitated solid was filtered and the filtrate evaporated on a rotary evaporator to remove all the solvents. The residue was dissolved in ethyl acetate (400 ml), washed with water (2×100 ml), brine (100 ml) and dried over anhydrous sodium sulfate and the solvent evaporated off. The crude product so obtained was chromatographed over silica gel (100-200 mesh) using chloroform as eluent to give 8.6 g (24.07%) of the title compound.

後処理

  1. stirringThe reaction mixture was stirred at the same temperature for 1 hour
  2. filtrationwas filtered
  3. customthe filtrate evaporated on a rotary evaporator
  4. customto remove all the solvents
  5. dissolutionThe residue was dissolved in ethyl acetate (400 ml)
  6. washwashed with water (2×100 ml), brine (100 ml)
  7. dry with materialdried over anhydrous sodium sulfate
  8. customthe solvent evaporated off
  9. customThe crude product so obtained
  10. customwas chromatographed over silica gel (100-200 mesh)

出典と根拠

ORDレコード
ord-7c614f2aee7249bf9c655e4d3705538f
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07691837B2

反応ノート

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