Acetic Acid → 4-Ethoxycarbonylfuran-2-carboxylic acid

HRID 332615

反応式

HRID 332615 の反応式
[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[CH:9][O:8][CH:7]=1)=[O:5])[CH3:2].BrBr.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(N(CC)CC)C.O.Cl.[C:41]([OH:44])(=[O:43])C>CN(C)C=O.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH2:1]([O:3][C:4]([C:6]1[CH:10]=[C:9]([C:41]([OH:44])=[O:43])[O:8][CH:7]=1)=[O:5])[CH3:2]

参加物

10

実験手順

3-Furancarboxylic acid ethyl ester (1.4 g, 10.0 mmol) was dissolved in acetic acid (10 mL), bromine (1.6 g, 10.0 mmol) was added, and the mixture was stirred overnight. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20). The obtained crude fraction was dissolved in N,N-dimethylformamide (15 mL), palladium acetate (0.18 g, 0.78 mmol), triphenylphosphine (0.41 g, 1.55 mmol), triethylamine (2.2 mL, 15.5 mmol), and water (0.7 mL, 38.8 mmol) were added, and the mixture was stirred at 80° C. overnight under a carbon monoxide atmosphere. 1N Hydrochloric acid was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The obtained residue was purified by high performance liquid chromatography to give the title compound (0.47 g).

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. customthe obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20)
  3. customThe obtained crude fraction
  4. stirringthe mixture was stirred at 80° C. overnight under a carbon monoxide atmosphere
  5. extractionthe mixture was extracted with ethyl acetate
  6. washThe extract was washed with saturated brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated under reduced pressure
  9. customThe obtained residue was purified by high performance liquid chromatography

出典と根拠

ORDレコード
ord-5357d541ba694a70b16c8446760eac70
出典データセット
uspto-grants-2014_11
特許番号
US08877805B2

関連ノート

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