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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988062Generated: October 25, 2026

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

https://huagongshe.com/reaction/1988062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Formylphenylboronic acidHCID 292189—
ReactantFuran, 2-bromo-HCID 2776190—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-(Furan-2-yl)benzaldehydeHCID 277229435.7%

Reaction Conditions

Temperature150 °C

Reaction Steps

A microwave vial (20 ml) was charged with 2-formylphenylboronic acid (298 mg, 2.0 mmol), 2-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 a crude material, which was purified by ISCO to give 123 mg of 2-furan-2-yl-benzaldehyde (34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553840B2
Source datasetuspto-grants-2009_06
ORD IDord-fb0ce5c6cf8546e4908ff9a2a4867118
Source noteuspto-grants-2009_06