HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422125Generated: October 25, 2026
Sodium Iodide → 1-Iodo-3-methoxy-5-methylbenzene
https://huagongshe.com/reaction/422125
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | 1-Bromo-3-methoxy-5-methylbenzene | HCID 10679554 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-Iodo-3-methoxy-5-methylbenzene | HCID 18719794 | 87% |
Reaction Steps
Cu(I)I (0.05 g, 0.25 mmol) and NaI (1.49 g, 10 mmol) were added to an oven dried sealed tube and the tube sealed with a rubber septum and flushed with a stream of nitrogen for 15 min. Anhydrous dioxane (5 mL), N,N′-dimethyl ethylenediamine (0.055 mL, 0.50 mmol) and 1-bromo-3-methoxy-5-methylbenzene (1) (1.0 g, 5.0 mmol) were added via a syringe with vigorous stirring under a stream of nitrogen at room temperature. The rubber septum was replaced with the Teflon cap and the sealed tube was heated at 110° C. in an oil bath for 18 h. The reaction was allowed to cool to room temperature and then quenched with a saturated aqueous solution of ammonium chloride. The reaction mixture was extracted with CH2Cl2. The organic layer was washed with water, and then concentrated to dryness to give 1-iodo-3-methoxy-5-methylbenzene (2) (1.05 g, 87% yield) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101605B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-73235beca452445b8809edfb891be59d |
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| Source note | uspto-grants-2012_01 |
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