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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815678Generated: October 30, 2026

Chlorobenzene → Biphenyl

https://huagongshe.com/reaction/1815678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductBiphenylHCID 709553%

Reaction Steps

A 30 mL of reactor equipped with magnetic stir bar was charged with 16 mg (0.022 mmol) of [(t-Bu)2P(Cl)PdCl2]2, 1.0 (8.8 mmol) of chlorobenzene, 1.3 g (10.66 mmol) of Ph—B(OH)2, 3.7 g (26.77 mmol) of K2CO3 in 5 mL of THF. The reaction mixture was refluxed for 4 hours. The reaction mixture was cooled to room temperature, transferred to a separatory funnel, and diluted with 220 mL of hexane and 150 mL of H2O. The layers were separated, and organic layer was washed with H2O (50 mL), brine (100 mL), and dried over MgSO4, filtered, and solvents removed from the filtrate by rotary evaporation. The resulting residue was chromatographed on silicon gel. The eluate was concentrated by rotary evaporation followed by high vacuum to give 0.72 g (53% yield) of biphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878850B2
Source datasetuspto-grants-2005_04
ORD IDord-8e0874654ac2432b8c81fd612c2ad634
Source noteuspto-grants-2005_04