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