3-Bromothiophene → 3-Bromothiophene-2-sulfonyl chloride
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
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- additionAfter the completion of addition
- customthe cold bath was removed
- additionThe reaction mixture was carefully added
- customdropwise, to crushed ice (100 g)
- extractionThe mixture was extracted with methylene chloride (2×100 ml)
- dry with materialThe combined organic layers was dried over MgSO4
- customevaporated
- customThe crude product was purified by flash chromatography on silica gel
Sources & evidence
- ORD record
- ord-79a30087cd614848ace3bffeaebb08c3
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331637B1
Reaction notes
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