3-Bromothiophene → 3-Bromothiophene-2-sulfonyl chloride

HRID 1841389Notes

Reaction equation

HRID 1841389 reaction equation
[Cl:1][S:2]([OH:5])(=O)=[O:3].[Br:6][C:7]1[CH:11]=[CH:10][S:9][CH:8]=1>C(Cl)Cl>[Br:6][C:7]1[CH:11]=[CH:10][S:9][C:8]=1[S:2]([Cl:1])(=[O:5])=[O:3]

Participants

4

Procedure

Chlorosulfonic acid (20 ml, 300 mmol) was added to a solution of 3-bromothiophene (8.15 g, 50 mmol) in methylene chloride (50 ml) at −78° C. over a 20 min. period. After the completion of addition, the cold bath was removed and stirring continued at ambient temperature for 1 hr. The reaction mixture was carefully added, dropwise, to crushed ice (100 g). The mixture was extracted with methylene chloride (2×100 ml). The combined organic layers was dried over MgSO4 and evaporated. The crude product was purified by flash chromatography on silica gel using hexane as the eluent resulting in 3-bromothiophene-2-sulfonyl chloride (4 g, 30% yield) and 4-bromothiophene-2-sulfonyl chloride (200 mg, ≦1%).

Workup

  1. additionAfter the completion of addition
  2. customthe cold bath was removed
  3. additionThe reaction mixture was carefully added
  4. customdropwise, to crushed ice (100 g)
  5. extractionThe mixture was extracted with methylene chloride (2×100 ml)
  6. dry with materialThe combined organic layers was dried over MgSO4
  7. customevaporated
  8. customThe crude product was purified by flash chromatography on silica gel

Sources & evidence

ORD record
ord-60d37f2459264862a3eedaf5be56b3de
Source dataset
uspto-grants-2004_01
Patent number
US06683103B2

Reaction notes

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