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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891956Generated: October 30, 2026

Water → 1-BROMO-5-METHOXYNAPHTHALENE

https://huagongshe.com/reaction/891956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfateHCID 6497—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromonaphthalen-1-olHCID 12336394—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventAcetonitrileHCID 6342—
Product1-BROMO-5-METHOXYNAPHTHALENEHCID 1090064964%

Reaction Steps

A suspension of 1-bromo-5-hydroxy-naphthalene (1.56 g, 7.0 mmol, prepared according to patent WO0146181), K2CO3 (1.45 g, 10.5 mmol), tetrabutylammonium chloride (15 mg, 0.05 mmol) and dimethyl sulfate (1.32 ml, 10.5 mmol) in MeCN was refluxed for 1 hour. After the addition of water, the aqueous phase was extracted three times with CH2Cl2. The combined organic layers were washed with water, dried over MgSO4, filtered and the solvent was removed under reduced to provide 1-bromo-5-methoxy-naphthalene (1.05 g, 64%) as a white solid, MS: m/e=236 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07005432B2
Source datasetuspto-grants-2006_02
ORD IDord-1183b18990504a3fa1b3198d4d7d073f
Source noteuspto-grants-2006_02