HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233481Generated: October 29, 2026
Sodium Carbonate → 2-(3-thienyl)benzaldehyde
https://huagongshe.com/reaction/2233481
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromothiophene | HCID 13383 | — |
| Reactant | 2-Formylphenylboronic acid | HCID 292189 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(3-thienyl)benzaldehyde | HCID 4321315 | 56% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709493B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-726541d01bc14c839bfad5f2ba54b07f |
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| Source note | uspto-grants-2010_05 |
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