HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Ethyl 7-(2-formyl-3-methoxyphenoxy)heptanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Methoxysalicylaldehyde | HCID 69692 | — |
| Reactant | Ethyl 7-bromoheptanoate | HCID 122490 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 7-(2-formyl-3-methoxyphenoxy)heptanoate | HCID 20271544 | — |
Reaction Steps
2-Hydroxy-6-methoxybenzaldehyde (3.04 g, 0.02 M), ethyl 7-bromoheptanoate (4.74 g, 0.02 M), anhydrous potassium carbonate (2.97 g), sodium iodide (0.12 g) and ethanol (27 ml) were refluxed with stirring for 19 hr. The cooled reaction mixture was filtered and the solid washed with ethanol. The filtrate was evaporated to dryness and the residue partitioned between ether (40 ml) and water (40 ml). The organic layer was separated and washed with ZN sodium hydroxide solution, water, dried (sodium sulphate) and evaporated to give ethyl 7-(2-formyl-3-methoxyphenoxy)heptanoate, 4.2 g, 68% as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04535183 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-2a8023f98b2841b287ce88a35ef8fafc |
| Source note | uspto-grants-1985_08 |