HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883600Generated: October 31, 2026
Methyl iodide → 7-Bromo-1-methoxynaphthalene
https://huagongshe.com/reaction/883600
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Bromonaphthalen-1-ol | HCID 13215711 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 7-Bromo-1-methoxynaphthalene | HCID 21865983 | 88.6% |
Reaction Steps
Potassium carbonate (3.3 g, 23.9 mmol) and methyl iodide (1.5 ml, 23.9 mmol) were added to a solution of the product from Step D (2.7 g, 11.9 mmol) in acetone (40 ml) at room temperature and the mixture was stirred at 65° C. for 2 hours. The solids were filtered, rinsed with ethyl acetate and the filtrate was evaporated. The residue was dissolved in ethyl acetate and washed with water twice. The aqueous layers were extracted with ethyl acetate. The combined organic extracts were washed with brine and dried over sodium sulfate to give 7-bromo-1-methoxynaphthalene (2.5 g, 88%) after chromatography (19:1 heptane/ethyl acetate): 1H NMR (300 MHz, CDCl3) δ 8.49 (d, J=2.1 Hz, 1H), 7.68 (d, J=8.7 Hz, 1H), 7.59 (dd, J=8.7, 2.1 Hz, 1H), 7.39-7.43 (m, 2H), 6.85 (dd, J=5.4, 3.0 Hz, 1H), 3.15 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236796B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-f835166d586940d293e4b851e3c7d8e4 |
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| Source note | uspto-grants-2012_08 |
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