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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426432Generated: October 29, 2026

Sodium Carbonate → 2-(Furan-3-yl)benzaldehyde

https://huagongshe.com/reaction/2426432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-BromofuranHCID 89164—
Reactant2-Formylphenylboronic acidHCID 292189—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-(Furan-3-yl)benzaldehydeHCID 1835761731.9%

Reaction Conditions

Temperature150 °C

Reaction Steps

A microwave vial (20 ml) was charged with 2-formylphenylboronic acid (298 mg, 2.0 mmol), 3-bromo-furan (350 mg, 2.4 mmol) and 8 ml of acetonitrile. To this mixture was added 4 ml of aqueous sodium carbonate (1M), followed by 100 mg of dichlorobis-(triphenylphosphine)-palladium(II). The reaction vessel was sealed and heated at 150° C. for 5 minutes with microwave irradiation. After cooling, the reaction mixture was extracted with ethylacetate. The organic layer was evaporated to provide crude material which was purified by ISCO to give 110 mg of 2-furan-3-yl-benzaldehyde (30% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968559B2
Source datasetuspto-grants-2011_06
ORD IDord-737a1bc85b93448ba89a447275dae2fb
Source noteuspto-grants-2011_06