Sodium hydride → HCID 53869820、化合物
反応式
[NH:1]1[CH:5]=[CH:4][N:3]=[N:2]1.[H-].[Na+].[H][H].[CH3:10][C:11]([CH3:25])([CH3:24])[C:12]([O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21]Br)=[CH:17][C:16]=1[Cl:23])=[O:13]>CN(C)C=O>[CH3:10][C:11]([CH3:25])([CH3:24])[C:12]([O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][N:2]2[N:3]=[CH:4][CH:5]=[N:1]2)=[CH:17][C:16]=1[Cl:23])=[O:13]参加物
反応条件
- 温度
- 10 °C
実験手順
A mixture of 2.26 g of 2H- 1,2,3-triazole, 1.31 g of sodium hydride (60% oil dispersion) and 100 ml of anhydrous N,N-dimethylformamide was stirred at 60° to 70° C. under a nitrogen atmosphere for 2 hours. After the evolution of hydrogen gas ceased, the mixture was cooled to 10° C. To this mixture was added dropwise an anhydrous N,N-dimethylformamide (150 ml) solution of 10 g of 4-bromomethyl-2-chlorophenyl 2,2-dimethylpropanoate at room temperature under stirring over 1 hour, and the mixture was stirred at 80° C. for 1 hour. After cooling, the reaction mixture was poured into ice water, which was extracted with ethyl acetate. The organic layer was washed with saturated aqueous ammonium chloride solution and then saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, which afforded 2-chloro-4-(2-2H-1,2,3-triazolyl)methylphenyl 2,2-dimethylpropanoate.
後処理
- stirringunder stirring over 1 hour
- stirringthe mixture was stirred at 80° C. for 1 hour
- temperatureAfter cooling
- extractionwas extracted with ethyl acetate
- washThe organic layer was washed with saturated aqueous ammonium chloride solution
- dry with materialsaturated sodium chloride solution, dried with anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-1d7e7f6dccec4fdfa8ddc7f9c5ba96b3
- 出典データセット
- uspto-grants-1999_10
- 特許番号
- US05972949
反応ノート
読み込み中…