HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378430Generated: October 26, 2026
2-Bromobiphenyl → 2-Phenylbenzene-1-sulfonyl chloride
https://huagongshe.com/reaction/378430
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromobiphenyl | HCID 16329 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Phenylbenzene-1-sulfonyl chloride | HCID 2756680 | 51.4% |
Reaction Steps
2-Bromobiphenyl (2.33 g, 10 mmol) was dissolved in ether (10 ml) and cooled to -78° C. n-Butyllithium (2.5 M solution in hexane, 4.8 ml, 12 mmol) was added dropwise under constant stirring and an argon atmosphere. The resultant reaction mixture was stirred at -70° C. to -60° C. for 1 h. The reaction mixture was cooled to -78° C. and sulfuryl chloride (0.88 ml, 11 mmol) was added dropwise. After addition, the reaction mixture was allowed to attain ambient temperature slowly and stirred for 1 h. The reaction mixture was diluted with ethyl acetate (50 ml), washed with water and the organic layer dried over anhydrous MgSO4. Removal of the solvent under reduced pressure gave a crude product, which was purified by column chromatography, using hexane followed by 5% ethyl acetate in hexane as eluent, to give 2-bi-phenylsulfonyl chloride as a solid (1.3 g, 51% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06030991 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-385d75d701174016b4efe36151d41bd1 |
|---|
| Source note | uspto-grants-2000_02 |
|---|