Methanol → 2-Methoxythiophene

HRID 723583노트

반응식

HRID 723583 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]=1

참가 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

  1. custom2-Methoxythiophene was prepared by the procedures
  2. temperaturewhile maintaining
  3. temperaturereflux
  4. temperaturethe mixture was maintained
  5. temperatureat reflux for 5.5 hours
  6. dissolutiondissolved
  7. extractionextracted with hexane
  8. dry with materialdried (Na2SO4)
  9. concentrationconcentrated to dryness
  10. distillationDistillation (90° C., 80 mm Hg)

출처 및 근거

ORD 기록
ord-d9c7b42e2aea4cf6aedc5fb6314d12b9
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07141584B2

반응 노트

불러오는 중…