HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 6-(5-Cholesten-3beta-yloxy)hexyl iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Cholest-5-en-3beta-yl 6-(p-toluenesulfonyloxy)hexyl ether | HCID 13799772 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 6-(5-Cholesten-3beta-yloxy)hexyl iodide | HCID 12805525 | — |
Reaction Steps
A solution of cholest-5-en-3β-yl 6-(p-toluenesulfonyloxy)hexyl ether (33 g, 51 mmol) and sodium iodide (16 g, 0.106 mol) in acetone (250 ml) was refluxed for 4 hours. The solvent was removed under reduced pressure, filtered, and the collected salts washed well with ether. The filtrate was evaporated and residual yellow oil boiled in hexanes (400 ml). The solution was decanted, concentrated to 200 ml, and stored in the refrigerator for two days. The product was filtered and the mother liquors concentrated to give a total yield of 30 g (97%), m.p. 103.5°-104.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04970199 |
| Source dataset | uspto-grants-1990_11 |
| ORD ID | ord-8098aa7318c1488a9262e475468fb7c6 |
| Source note | uspto-grants-1990_11 |