Methanol → Methyl 5-bromothiophene-3-carboxylate

HRID 238276

반응식

HRID 238276 반응식
[Br:1][C:2]1[S:6][CH:5]=[C:4]([C:7]([OH:9])=[O:8])[CH:3]=1.S(=O)(=O)(O)O.[CH3:15]O>>[CH3:15][O:8][C:7]([C:4]1[CH:3]=[C:2]([Br:1])[S:6][CH:5]=1)=[O:9]

참가 물질

4

실험 절차

5-Bromo-thiophene-3-carboxylic acid (13 g, 64 mmol) was dissolved in methanol (140 mL). Concentrated sulphuric acid (6.5 mL) was added and the mixture heated at reflux for 14 hours. The reaction was quenched by adding a solution of saturated aqueous sodium bicarbonate and most of the solvent was removed by evaporation under vacuum. The mixture was then diluted with a solution of saturated aqueous sodium bicarbonate and the product extracted with DCM. The organic solution was dried over sodium sulphate, filtered and the solvent removed by evaporation to give a white crystalline solid (13.2 g). 1H NMR (400 MHz, CDCl3): δ 8.0 (s, 1H), 7.5 (s, 1H), 3.85 (s, 3H).

후처리

  1. temperaturethe mixture heated
  2. temperatureat reflux for 14 hours
  3. customThe reaction was quenched
  4. additionby adding a solution of saturated aqueous sodium bicarbonate
  5. custommost of the solvent was removed by evaporation under vacuum
  6. additionThe mixture was then diluted with a solution of saturated aqueous sodium bicarbonate
  7. extractionthe product extracted with DCM
  8. dry with materialThe organic solution was dried over sodium sulphate
  9. filtrationfiltered
  10. customthe solvent removed by evaporation

출처 및 근거

ORD 기록
ord-b9da8d2ffc3b4b689872ff25615d0d33
출처 데이터셋
uspto-grants-2014_02
특허 번호
US08642621B2

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