HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-Ethoxy-3-fluoro-5-iodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Tosylchloramide | HCID 31388 | — |
| Reactant | 3-Ethoxy-5-fluorophenylboronic Acid (contains varying amounts of Anhydride) | HCID 44558175 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Ethoxy-3-fluoro-5-iodobenzene | HCID 67324085 | — |
Reaction Steps
(3-Ethoxy-5-fluorophenyl)boronic acid (2.5 g, 0.014 mol) was dissolved in THF (30 mL) and a solution of sodium iodide (4.1 g, 0.028 mol) in H2O (15 mL) was added followed by a solution of chloramine T (7.8 g, 0.1 mol) in H2O (15 mL). After 20 h stirring, the reaction mixture was extracted with diethylether (3×50 mL). The organic layers were combined and the solvent was evaporated. The resulting residue was triturated with hexanes (3×) and the hexanes layers were combined. The solvent was evaporated to yield 1-fluoro-3-iodo-5-ethoxybenzene as an orange oil. The product was used in the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765779B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-d24e001545984dbd80bd1dc1c64c4c0d |
| Source note | uspto-grants-2014_07 |