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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1433853Generated: October 25, 2026

Ammonia → 2-Methoxy-6-(4-methoxy-2-nitrophenyl)naphthalene

https://huagongshe.com/reaction/1433853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantLithium ChlorideHCID 433294—
ReactantTributyl(4-methoxy-2-nitrophenyl)tinHCID 23087474—
CatalystCuprous chlorideHCID 62652—
CatalystHCID 178418397HCID 178418397—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Product2-Methoxy-6-(4-methoxy-2-nitrophenyl)naphthaleneHCID 2308755663.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

The title compound was synthesized by referring to J. Am. Chem. Soc., 1999, 121, 760. A suspension of 6-methoxy-2-bromonaphthalene (500 mg), tributyl(4-methoxy-2-nitrophenyl)tin (1.1 g), tetrakis(triphenylphosphine)palladium(0) (250 mg), copper(I) chloride (1.0 g) and lithium chloride (540 mg) in dimethylsulfoxide (15 ml) was stirred at 60° C. for 5 hours under a nitrogen atmosphere. Ethyl acetate and aqueous ammonia were sequentially added thereto, the solution was filtered through celite pad, extracted with ethyl acetate, then sequentially washed with water and brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was washed with a hexane-diethyl ether system to provide the title compound (412 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-8387e951015b4c6db75044133ccf01bd
Source noteuspto-grants-2009_11