2,4-Dimethylbenzoic acid → Methyl 2,4-dimethylbenzoate

HRID 1625870

反応式

HRID 1625870 の反応式
[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:12](Cl)(=O)C(Cl)=O>C(Cl)(Cl)Cl.CN(C)C=O>[CH3:1][C:2]1[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:12])=[O:5]

参加物

5

実験手順

2,4-dimethylbenzoic acid (20.0 g) was suspended in chloroform (100 ml), and thereto were added oxalyl chloride (6.8 ml) and N,N-dimethylformamide (2 drops). The mixture was stirred at room temperature overnight. The solvent was evaporated under reduced pressure, and the residue was dissolved in methanol (200 ml). The mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate. The mixture was washed successively with a saturated aqueous sodium hydrogen carbonate solution and brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure to give methyl 2,4-dimethylbenzoate as pale yellow oil, which was used in the subsequent step without further purification.

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. dissolutionthe residue was dissolved in methanol (200 ml)
  3. stirringThe mixture was stirred at room temperature for 3 hours
  4. customThe solvent was evaporated under reduced pressure
  5. dissolutionthe residue was dissolved in ethyl acetate
  6. washThe mixture was washed successively with a saturated aqueous sodium hydrogen carbonate solution and brine
  7. dry with materialdried over sodium sulfate
  8. customThe solvent was evaporated under reduced pressure

出典と根拠

ORDレコード
ord-b9fa98f2bcf44b5cabbfc1ecb919a6f0
出典データセット
uspto-grants-2014_07
特許番号
US08785403B2

関連ノート

読み込み中…