反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([SH:9])[CH:6]=[CH:7][CH:8]=1.[C:10](Cl)(=[O:14])[C:11](Cl)=[O:12].[Cl-].[Al+3].[Cl-].[Cl-]>CCOCC>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]2[C:10](=[O:14])[C:11](=[O:12])[S:9][C:5]=2[CH:4]=1参加物
実験手順
To a solution of 3-methoxythiophenol (3.75 g, 26.7 mmol) in ether (20 mL) was added oxalyl chloride (3.7 mL, 43 mmol) dropwise. The mixture was heated at reflux for 1.5 h, cooled to rt, and concentrated in vacuo. The resulting yellow oil was dissolved in dichloromethane (50 mL), cooled to 0° C., and was treated with aluminum chloride (4.30 g, 32.0 mmol) in portions. The mixture was heated at reflux for 30 min, cooled to rt, and poured onto ice water with stirring. The organic layer was separated and successively washed with saturated, aqueous sodum bicarbonate, water, and brine. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by chromatography (4/1 ethyl acetate/hexane) which provided 2.46 g (47%) of 6-methoxy-1-benzothiophene-2,3-dione as an orange solid.
後処理
- temperatureThe mixture was heated
- temperatureat reflux for 1.5 h
- concentrationconcentrated in vacuo
- dissolutionThe resulting yellow oil was dissolved in dichloromethane (50 mL)
- temperaturecooled to 0° C.
- temperatureThe mixture was heated
- temperatureat reflux for 30 min
- temperaturecooled to rt
- additionpoured onto ice water
- customThe organic layer was separated
- washsuccessively washed with saturated, aqueous sodum bicarbonate, water, and brine
- dry with materialThe organic layer was dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by chromatography (4/1 ethyl acetate/hexane) which
出典と根拠
- ORDレコード
- ord-7b4b5dc5d57c4724a2802c423685f17d
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07429664B2
関連ノート
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