HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromothiophene → 3-Bromothiophene-2-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromothiophene | HCID 13383 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromothiophene-2-sulfonyl chloride | HCID 13675598 | 30.6% |
Reaction Steps
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%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05962490 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-c67c053fa06f4697b9371084f66cf4af |
| Source note | uspto-grants-1999_10 |