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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 883600Generated: October 31, 2026

Methyl iodide → 7-Bromo-1-methoxynaphthalene

https://huagongshe.com/reaction/883600

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 numberUS08236796B2
Source datasetuspto-grants-2012_08
ORD IDord-f835166d586940d293e4b851e3c7d8e4
Source noteuspto-grants-2012_08