HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Ethyl 2-(6-iodohexyloxy)-2-methylpropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethyl 2-(6-bromohexyloxy)-2-methylpropionate | HCID 21866767 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 2-(6-iodohexyloxy)-2-methylpropionate | HCID 21866667 | 102.6% |
Reaction Steps
To 76 ml of a solution of 12.16 g of ethyl 2-(6-bromohexyloxy)-2-methylpropionate in acetone, 18.52 g of sodium iodide was added, and heated to reflux for 18 hours. The reaction solution was cooled, filtered to remove insolubles and washed with acetone. The filtrate was concentrated and, after addition of water, extracted with ethyl acetate. The organic layer was washed with water and brine sequentially, dried over anhydrous magnesium sulfate and concentrated to provide 14.46 g of the objective compound as red-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06998412B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-5dc6ffaf47844884b13b36a58dc565d4 |
| Source note | uspto-grants-2006_02 |