Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221387Generated: October 31, 2026

Bromobenzene → 2,4-Difluoro-1,1'-biphenyl

https://huagongshe.com/reaction/221387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantSodium CarbonateHCID 10340—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2,4-Difluoro-1,1'-biphenylHCID 169974—

Reaction Conditions

Temperature90 °C

Reaction Steps

2,4-Difluorophenylboronic acid (15 g, 129 mmol) was added to a solution of bromobenzene (19.8 g, 126 mmol) in DME (500 mL). To this was added a solution of sodium carbonate (55.8 g, 520 mmol) in water (260 mL). The solution was degassed by bubbling argon through the mixture and then stirred under argon. Pd(dppf)Cl2 (1.5 g, 2.1 mmol) was added and the flask was flushed with argon and heated at 90° C. overnight. The mixture was then cooled to room temperature and water (150 mL) and ethyl acetate (500 mL) were added. The layers were separated and the organic layer washed with 2 M NaOH (100 mL), water (100 mL) and brine (100 mL). The black ethyl acetate layer was dried over MgSO4, charcoal was added, and the mixture was filtered through a short pad of silica. Evaporation of the solvents gave 2,4-difluorobiphenyl as a brown oil, which crystallised on standing (21.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207167B2
Source datasetuspto-grants-2012_06
ORD IDord-1e2b3341fa654e64ab012fc4bfc0d3c5
Source noteuspto-grants-2012_06