반응식
[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]=1참가 물질
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-7b4b5dc5d57c4724a2802c423685f17d
- 출처 데이터셋
- uspto-grants-2008_09
- 특허 번호
- US07429664B2
연결된 노트
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