Methanol → Methyl 5-bromothiophene-3-carboxylate

HRID 238276

Reaction equation

HRID 238276 reaction equation
[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]

Participants

4

Procedure

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).

Workup

  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

Sources & evidence

ORD record
ord-b9da8d2ffc3b4b689872ff25615d0d33
Source dataset
uspto-grants-2014_02
Patent number
US08642621B2

Linked notes

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