Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobiphenylHCID 16329—
ReactantSulfuryl chlorideHCID 24648—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product2-Phenylbenzene-1-sulfonyl chlorideHCID 275668051.4%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030991
Source datasetuspto-grants-2000_02
ORD IDord-385d75d701174016b4efe36151d41bd1
Source noteuspto-grants-2000_02