HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 2-(p-Methoxybenzoyl)-3-methyl-4-allyloxybenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(p-Methoxybenzoyl)-3-methyl-4-hydroxybenzofuran | HCID 14579791 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(p-Methoxybenzoyl)-3-methyl-4-allyloxybenzofuran | HCID 15029668 | — |
Reaction Steps
A mixture of 2-(p-methoxybenzoyl)-3-methyl-4-hydroxybenzofuran (0.60 gm; 2.2 mmoles), potassium carbonate (0.83 gm; 6.0 mmoles) and allyl bromide (0.73 gm; 6.0 mmoles) in acetone (25 mL) was refluxed for a period of 22 hours. The reaction mixture was cooled, filtered through Celite, and concentrated in vacuo. The residue was chromatographed on silica gel using 15% ethylacetate in hexane as eluent to yield 2-(p-methoxybenzoyl)-3-methyl-4-allyloxybenzofuran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863958 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-d4cbadfd5a6e414e943a3b047199d3b1 |
| Source note | uspto-grants-1989_09 |