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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403461Generated: November 2, 2026

Bromobenzene → 2-Phenylfuran

https://huagongshe.com/reaction/1403461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantFuran-2-boronic acidHCID 2734357—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-PhenylfuranHCID 51936362.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of (furan-2-yl)boronic acid (3.0 g, 26.81 mmol) in dioxane (50.0 mL) and water (1.0 mL) was added bromobenzene (2.10 g, 13.38 mmol), K3PO4 (9.3 g, 43.81 mmol) and Pd(PPh3)4 (767 mg, 0.66 mmol) with stirring for 3 h at 95° C. in an oil bath under an inert atmosphere of nitrogen. The reaction mixture was concentrated under reduced pressure to give the residue, which was purified by silica gel column chromatography (1% ethyl acetate in petroleum ether) to afford 2-phenylfuran as colorless oil (1.20 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-739e8501afdd4f57823d31bee8d99dc7
Source noteuspto-grants-2014_12