HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Ethyl 5-(2-formyl-3-benzyloxyphenoxy)pentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | 2-(Benzyloxy)-6-hydroxybenzaldehyde | HCID 14162879 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 5-(2-formyl-3-benzyloxyphenoxy)pentanoate | HCID 20271552 | 86% |
Reaction Steps
A mixture of 2-hydroxy-6-benzyloxybenzaldehyde (3.0 g, 0.013 M), ethyl 5-bromopentanoate (2.75 g, 0.013 M), anhydrous potassium carbonate (2.16 g, 0.0156 M), sodium iodide (0.195 g) and dry dimethylformamide (15 ml) were stirred at 60°-80° c. for 3 hours and then left to stir at room temperature overnight. The mixture was then poured into water (50 ml) and the product extracted with ether (2×80 ml) and the combined extracts washed with 10% aqueous sodium hydroxide (2×20 ml) and then with water to neutrality, dried, and evaporated to give ethyl 5-(2-formyl-3-benzyloxyphenoxy)pentanoate, (4.0 g, 86%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04410537 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-62eab3993fce482e825e10c69a677cf2 |
| Source note | uspto-grants-1983_10 |