HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Bromo-7-methoxy-1-benzofuran-2-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 7-Methoxy-1-benzofuran-2-carbaldehyde | HCID 3457310 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-7-methoxy-1-benzofuran-2-carbaldehyde | HCID 18784864 | — |
Reaction Steps
2-Formyl-7-methoxybenzofuran (1.0 g) was stirred in dichloromethane (10 ml) under nitrogen at 0° C. Sodium acetate (1.4 g) was added followed by the dropwise addition of bromine (0.29 ml). Further dichloromethane (20 ml) was added to the mixture to facilitate stirring and the mixture was stirred overnight. The reaction mixture was diluted with dichloromethane (40 ml) and washed with water (30 ml). Drying over magnesium sulfate followed by removal of the solvent in vacuo gave a pale orange solid. Purification by flash chromatography on silica eluting with 10% ethyl acetate in hexane gave the title compound (0.50 g) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06066657 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-7eb9a6b965734d07987a37983b422353 |
| Source note | uspto-grants-2000_05 |