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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823940Generated: October 30, 2026

Potassium Carbonate → 5-(2-methylphenyl)furan-2-carbaldehyde

https://huagongshe.com/reaction/1823940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromofuran-2-carbaldehydeHCID 600328—
Reactant2-Methylphenyl boronic acidHCID 2733267—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-(2-methylphenyl)furan-2-carbaldehydeHCID 467482484.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

As illustrated in Scheme 1, to a mixture of 5-bromo-2-furaldehyde (2.0 g, 11.4 mmol), tetrabutylammonium bromide (3.7 g, 11.4 mmol), potassium carbonate (3.93 g, 28.5 mmol), 2-methylphenyl boronic acid (1.7 g, 12.5 mmol) and palladium (II) acetate (55.2 mg, 0.23 mmol) is added water (20 mL). The reaction mixture is then stirred vigorously for 16 hour at 25° C. Once complete, the reaction mixture is poured into a separatory funnel and diluted with water (50 mL) and ethyl acetate (150 mL). The organic layer is separated and treated with 5.0 g of activated charcoal for 30 min after which time the suspension is filtered through a pad of celite and the filtrate concentrated to afford the crude coupling product as a yellow oil. The crude product is purified by column chromatography (5→10% ethyl acetate in hexanes) to afford 1.8 g of 5-(2′-methylphenyl)-2-furaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041690B2
Source datasetuspto-grants-2006_05
ORD IDord-47a93ed042064c049795a29034a68b77
Source noteuspto-grants-2006_05