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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromofuran | HCID 89164 | — |
| Reactant | 2-Formylphenylboronic acid | HCID 292189 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Furan-3-yl)benzaldehyde | HCID 18357617 | 31.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07968559B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-737a1bc85b93448ba89a447275dae2fb |
|---|
| Source note | uspto-grants-2011_06 |
|---|