反応式
[CH3:1][O:2][CH:3](O)[CH2:4][CH3:5].[H-].[Na+].Cl[C:10]1[C:15]([CH3:16])=[CH:14][N+:13]([O-:17])=[C:12]([CH3:18])[C:11]=1[CH3:19].CS(C)=[O:22]>>[CH3:1][O:2][CH2:3][CH2:4][CH2:5][O:22][C:10]1[C:15]([CH3:16])=[CH:14][N+:13]([O-:17])=[C:12]([CH3:18])[C:11]=1[CH3:19]参加物
反応条件
- 温度
- 60 °C
実験手順
4.5 g (0.05 mol) of methoxypropanol was dissolved in 45 ml of dimethyl sulfoxide to obtain a solution. 2.0 g of 60% sodium hydride was added to this solution at a room temperature in a nitrogen atmosphere. The obtained mixture was heated to 60° C. and stirred for one hour. After the completion of the reaction, a solution of 4.3 g (0.025 mol) of 4-chloro-2,3,5-trimethylpyridine 1-oxide in 15 ml of dimethyl sulfoxide was dropwise added to the reaction mixture at a room temperature. The obtained mixture was stirred at 60° C. for 5 hours, cooled and distilled to dryness to remove the solvent. 200 ml of water was added to the obtained residue. The obtained mixture was extracted with 150 ml of chloroform five times. The extract was dried over magnesium sulfate and filtered. The filtrate was distilled to remove the solvent. The residue was purified by silica gel column chromatography (ethyl acetate/n-hexane) to obtain 4.27 g of the title compound as an oil.
後処理
- customto obtain a solution
- customAfter the completion of the reaction
- stirringThe obtained mixture was stirred at 60° C. for 5 hours
- temperaturecooled
- distillationdistilled to dryness
- customto remove the solvent
- addition200 ml of water was added to the obtained residue
- extractionThe obtained mixture was extracted with 150 ml of chloroform five times
- dry with materialThe extract was dried over magnesium sulfate
- filtrationfiltered
- distillationThe filtrate was distilled
- customto remove the solvent
- customThe residue was purified by silica gel column chromatography (ethyl acetate/n-hexane)
出典と根拠
- ORDレコード
- ord-1d58406a8b994aa7b63e9078ecd96c75
- 出典データセット
- uspto-grants-1998_11
- 特許番号
- US05840910
関連ノート
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