HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Ethyl 6-iodohexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 6-iodohexanoate | HCID 10880140 | 100.1% |
Reaction Steps
To 112 ml of a solution of 13.38 g of ethyl 6-bromohexanoate in acetone, 26.97 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 16.21 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-f7d2d449ab684d619322406385f1a335 |
| Source note | uspto-grants-2006_02 |