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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Formylphenylboronic acid | HCID 292189 | — |
| Reactant | Furan, 2-bromo- | HCID 2776190 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Furan-2-yl)benzaldehyde | HCID 2772294 | 35.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07553840B2 |
|---|
| Source dataset | uspto-grants-2009_06 |
|---|
| ORD ID | ord-fb0ce5c6cf8546e4908ff9a2a4867118 |
|---|
| Source note | uspto-grants-2009_06 |
|---|