HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Ethyl 7-allyloxynaphthalene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 7-hydroxynaphthalene-2-carboxylate | HCID 12635629 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 7-allyloxynaphthalene-2-carboxylate | HCID 20282953 | 81% |
Reaction Steps
A mixture of ethyl 7-hydroxynaphthalene-2-carboxylate (37.5 g), anhydrous potassium carbonate (24.0 g), potassium iodide (0.5 g), and allyl bromide (29.0 g) was heated in refluxing acetone (200 ml) with stirring for 15 hours. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in ethyl-acetate, washed with 2% sodium hydroxide solution and water, dried and evaporated to give a solid. Crystallisation from petroleum ether (b.p. 40-60) afforded ethyl 7-allyloxynaphthalene-2-carboxylate (36 g), m.p. 60°-61°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518612 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-010ec888aa54404db7f6eec6f76e531c |
| Source note | uspto-grants-1985_05 |