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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983896Generated: November 2, 2026

Methyl iodide → 7-Bromo-1-methoxynaphthalene

https://huagongshe.com/reaction/1983896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Bromonaphthalen-1-olHCID 13215711—
SolventAcetoneHCID 180—
Product7-Bromo-1-methoxynaphthaleneHCID 2186598388.6%

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07541357B2
Source datasetuspto-grants-2009_06
ORD IDord-bf6d2692a05c4ea09a0954e1878f1c3d
Source noteuspto-grants-2009_06