Methanol → 2-Methoxythiophene
반응식
[Na].Br[C:3]1[S:4][CH:5]=[CH:6][CH:7]=1.[C-]#N.[Na+:10].[CH3:11][OH:12]>O>[CH3:11][O-:12].[Na+:10].[CH3:11][O:12][C:3]1[S:4][CH:5]=[CH:6][CH:7]=1참가 물질
7
실험 절차
2-Methoxythiophene was prepared by the procedures described in H. A. Keeystra et al., Tetrahedron, 1992, 48, 3633. Thus, a solution of sodium methoxide in methanol was prepared by adding sodium (2.12 g, 92.2 mmol) to methanol (14 ml). 2-Bromothiophene (10 g, 61.3 mmol) was added while maintaining reflux. Cuprous bromide (0.88 g, 6.1 mmol) was added and the mixture was maintained at reflux for 5.5 hours. A solution of sodium cyanide (3 g, 61.3 mmol) in water (30 ml) was added at 20–25° C. under vigorous stirring. The mixture was stirred until all solids dissolved, extracted with hexane, dried (Na2SO4), and concentrated to dryness. Distillation (90° C., 80 mm Hg) gave 2-methoxythiophene (5.35 g, 76%) as a colorless oil.
후처리
- custom2-Methoxythiophene was prepared by the procedures
- temperaturewhile maintaining
- temperaturereflux
- temperaturethe mixture was maintained
- temperatureat reflux for 5.5 hours
- dissolutiondissolved
- extractionextracted with hexane
- dry with materialdried (Na2SO4)
- concentrationconcentrated to dryness
- distillationDistillation (90° C., 80 mm Hg)
출처 및 근거
- ORD 기록
- ord-d9c7b42e2aea4cf6aedc5fb6314d12b9
- 출처 데이터셋
- uspto-grants-2006_11
- 특허 번호
- US07141584B2
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