HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-Bromo-2-(4-methoxybenzyl)benzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-Bromo-2-(4-methoxybenzoyl)benzofuran | HCID 2371724 | — |
| Reactant | Hydrazine--water (1/2) | HCID 22141362 | — |
| Solvent | Diethylene Glycol | HCID 8117 | — |
| Product | 5-Bromo-2-(4-methoxybenzyl)benzofuran | HCID 21844370 | 82.5% |
Reaction Steps
5.07 g of potassium hydroxide was added to 30 ml of diethylene glycol, and the mixture was stirred at room temperature during which 5.5 g of 80% hydrazine dihydrate.2H2O and 5.0 g of 5-bromo-2-(4-methoxybenzoyl)benzofuran were further added. The thus prepared mixture was refluxed under heating. After cooling, the resulting reaction solution was adjusted to pH 4-5, extracted with benzene, and then dried. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a n-hexane/isopropanol mixture as an elution solvent, thereby obtaining 3.95 g of 5-bromo-2-(4-methoxybenzyl)benzofuran as a brown oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05576343 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-d829c7ee9fbc42eab859867b19cfd640 |
| Source note | uspto-grants-1996_11 |