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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402112Generated: November 2, 2026

Methyl iodide → 7-Bromo-1-methoxynaphthalene

https://huagongshe.com/reaction/402112

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 numberUS08741901B2
Source datasetuspto-grants-2014_06
ORD IDord-e9957a812650489c8efdb2b7e87cd4e6
Source noteuspto-grants-2014_06