HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899709Generated: October 31, 2026
3-Bromobiphenyl → 3-Phenylbenzene-1-sulfonyl chloride
https://huagongshe.com/reaction/1899709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromobiphenyl | HCID 16449 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Phenylbenzene-1-sulfonyl chloride | HCID 3802752 | 49.5% |
Reaction Steps
3-Bromobiphenyl (1.5 g, 6.4 mmol) was dissolved in ether (15 ml) and cooled to -78° C. t-Butyllithium (1.7M solution in hexane, 3.8 ml, 6.4 mmol) was added dropwise under constant stirring and an argon atmosphere. The resultant reaction mixture was stirred at -10° C. to -5° C. for 6 h. The reaction mixture was cooled to -78° C. and sulfuryl chloride (0.64 ml, 6.4 mmol) was added dropwise. After the completion of the 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 crude product, which was purified by column chromatography, using hexane followed by 5% ethyl acetate in hexane as eluent, to give 3-biphenylsulfonyl chloride as a oil (0.8 g, 49% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571821 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-12d78b4f748e4257907e48df1bd5f54f |
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| Source note | uspto-grants-1996_11 |
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