HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Ethyl 4-allyloxy-3-methylbenzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-hydroxy-3-methyl-1-benzofuran-2-carboxylate | HCID 748649 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 4-allyloxy-3-methylbenzofuran-2-carboxylate | HCID 13849488 | 92.2% |
Reaction Steps
A mixture of ethyl-4-hydroxy-3-methylbenzofuran-2-carboxylate (11.0 g, 50 mmol), allyl bromide (4.8 ml, 55 mmol) and potassium carbonate (55 mmol) was refluxed in acetone (300 ml) for 4 hours. The resulting mixture was cooled, filtered and concentrated. The residue was chromatographed (silica gel, eluted with 5% ethyl acetate in hexane) to give 12 g of the title compound, m.p. 64°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04663347 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-9f06f4d69168453a8e7b43c686f602f6 |
| Source note | uspto-grants-1987_05 |