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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634247Generated: October 31, 2026

Benzene → Biphenyl

https://huagongshe.com/reaction/1634247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium CarbonateHCID 10340—
CatalystTetrabutylammonium BromideHCID 74236—
ProductBiphenylHCID 7095—

Reaction Steps

The residue was dissolved in benzene and then there was added tetrabutylammonium bromide, aqueous Na2CO3 and 2-(tert-butylaminosulfonyl)phenylboronic. This solution was degassed with a stream of nitrogen for 30 minutes. Following the purge, tetrakis(triphenylphosphine)palladium(0) was added and the solution was stirred overnight at reflux. The solution was diluted with EtOAc and washed twice with brine and the organics dried over MgSO4, filtered and the volatiles removed under reduced pressure. The residue was purified by column chromatography (elution with 1:1 hexane/EtOAc) to afford an intermediate biphenyl compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506771B2
Source datasetuspto-grants-2003_01
ORD IDord-8a2dfa75b30c472388fb4ad94f9403b8
Source noteuspto-grants-2003_01