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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620865Generated: October 31, 2026

Sodium Carbonate → 2-(3-thienyl)benzaldehyde

https://huagongshe.com/reaction/1620865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-BromothiopheneHCID 13383—
Reactant2-Formylphenylboronic acidHCID 292189—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product2-(3-thienyl)benzaldehydeHCID 432131556%

Reaction Conditions

Temperature150 °C

Reaction Steps

A microwave vial (20 ml) was charged with 2-formylphenylboronic acid (290 mg, 2.0 mmol), 3-bromo-thiophene (326 mg, 2.0 mmol), and 8 ml of acetonitrile. To this mixture was added 4 ml of aqueous sodium carbonate (1M), followed by 50 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 211 mg of 2-thiophen-3-yl-benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772482B2
Source datasetuspto-grants-2014_07
ORD IDord-48d422de6683441994a93fdadeb354bc
Source noteuspto-grants-2014_07