HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261094Generated: November 3, 2026
Potassium Hydroxide → 3-Bromo-benzofuran-5-carbaldehyde
https://huagongshe.com/reaction/2261094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dibromo-2,3-dihydro-1-benzofuran-5-carbaldehyde | HCID 57469664 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-benzofuran-5-carbaldehyde | HCID 57469663 | 96.5% |
Reaction Steps
To a solution of 2,3-dibromo-2,3-dihydro-1-benzofuran-5-carbaldehyde (4.1 g) in dry ethanol (15 mL) was added a solution of KOH (2.2 eq.) in dry ethanol (14 mL) and refluxed at 70° C. for 1 h. The reaction mixture was cooled, diluted with water and extracted with EtOAc (3×50 mL). The organic layer was washed with water, brine and dried. The solvent was removed under vacuum and the residue was purified by flash chromatography (pet. ether/EtOAc 99.5:0.5) to give the title compound as a pale yellow solid (2.91 g (80% pure), yield=78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07846925B2 |
|---|
| Source dataset | uspto-grants-2010_12 |
|---|
| ORD ID | ord-536903aa5f574ebc9f6f46b5770fc5cd |
|---|
| Source note | uspto-grants-2010_12 |
|---|