Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-(2-Naphthyloxy)ethyl 4-Bromobenzenesulfonate | HCID 18669132 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2-Iodoethoxy)naphthalene | HCID 18669165 | 72.1% |
Reaction Steps
To a solution of 2-(2-naphthyloxy)ethyl 4-bromobenzenesulfonate (Preparation 10, 380 mg, 0.93 mmol) in acetone (5 mL) at room temperature was added sodium iodide (1.0 g, 6.66 mmol). The mixture was heated at 35° C. for 16 hours and then cooled. The residual precipitate was removed by filtration and the filtrate was concentrated in vacuo. The residue was partitioned between diethyl ether (20 mL) and water (20 mL). The two layers were separated and the organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to give the title compound (200 mg, 72%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518282B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-def6471ed8d94e25a99e0548e444ee9d |
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| Source note | uspto-grants-2003_02 |
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