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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950039Generated: October 26, 2026

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

https://huagongshe.com/reaction/1950039

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 numberUS08399520B2
Source datasetuspto-grants-2013_03
ORD IDord-54e0a600cc4941f8a3d85b5e479c0410
Source noteuspto-grants-2013_03