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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504488Generated: October 31, 2026

2-Methoxynaphthalene → 2-Bromo-3-methoxynaphthalene

https://huagongshe.com/reaction/1504488

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxynaphthaleneHCID 7119—
Reactant1,2-DibromoethaneHCID 7839—
ReactantSodium HydroxideHCID 14798—
ReactantButyllithiumHCID 178418339—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-3-methoxynaphthaleneHCID 1335191058.4%

Reaction Steps

A RBF was charged 2-methoxynaphthalene (2.00 g, 12.64 mmol) and THF (30 mL) to give a clear solution. n-butyllithium (2.5M in hexanes) (5.66 mL, 14.16 mmol) was added dropwise. The flask was cooled in a dry ice-acetone bath for 10 min and 1,2-dibromoethane (1.634 mL, 18.96 mmol) was added dropwise. The reaction was warmed to room temperature and stirred for 16 hours. NaOH (1 M, 10 mL, 10 mmol 0 was added and the reaction was heated to reflux for 1 hour. The mixture was cooled to room temperature and extracted with DCM (2×), and the combined organic extracts were dried over magnesium sulfate, filtered, and concentrated. The crude solid was recrystallized from heptane to give 2-bromo-3-methoxynaphthalene (1.75 g, 7.38 mmol, 58.4% yield) as an off-white solid. m/z (ESI) 237.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212182B2
Source datasetuspto-grants-2015_12
ORD IDord-f7dc892d457d434698b64d65e527b2d9
Source noteuspto-grants-2015_12