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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896474Generated: October 25, 2026

Potassium Carbonate → 5-Phenyl-2-furaldehyde

https://huagongshe.com/reaction/896474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromofuran-2-carbaldehydeHCID 600328—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product5-Phenyl-2-furaldehydeHCID 2769420—

Reaction Steps

A solution of 5-bromo-furan-2-carbaldehyde (1.08 g, 6.16 mmol, 1 eq), phenylboronic acid (0.90 g, 7.39 mmol, 1.1 eq), tetrabutylammonium bromide (1.99 g, 6.16 mmol, 1 eq), palladium acetate (30 mg, 0.0.12 mmol 0.02 eq), K2CO3 (2.13 g, 15.4 mmol, 2.5 eq) in water (10 mL) is stirred under nitrogen at rt overnight. The reaction is diluted with 40 mL water and extracted with EtOAc (3×100 mL). The organic layers are combined and stirred with charcoal for 30 min, then dried over MgSO4 and filtered. The solvent is removed under reduced pressure to give 5-phenyl-furan-2-carbaldehyde as an oil. The product is purified by silica gel chromatography using a Biotage Flash 40M column (10% EtOAc/heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919359B2
Source datasetuspto-grants-2005_07
ORD IDord-98b5835f61b24615b76ebd54d47bdad3
Source noteuspto-grants-2005_07