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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263650Generated: November 1, 2026

3-Bromobiphenyl → 3-Phenylbenzene-1-sulfonyl chloride

https://huagongshe.com/reaction/1263650

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromobiphenylHCID 16449—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 178418306HCID 178418306—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product3-Phenylbenzene-1-sulfonyl chlorideHCID 380275249.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-Bromobiphenyl (1.5 g, 6.4 mmol) was dissolved in ether (15 ml) and cooled to −78° C. t-Butyllithium (1.7 M 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 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 an oil (0.8 g, 49% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541498B2
Source datasetuspto-grants-2003_04
ORD IDord-403a310393324113a4418abacdfca071
Source noteuspto-grants-2003_04