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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893551Generated: November 2, 2026

Iodoethane → 3-Methoxynaphthalen-2-amine

https://huagongshe.com/reaction/1893551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium HydroxideHCID 14798—
ReactantSodium hydrideHCID 24758—
Reactant3-Amino-2-naphtholHCID 79449—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Methoxynaphthalen-2-amineHCID 23514152.3%

Reaction Steps

3-Amino-2-naphthol (7.96 g, 50.0 mmol) was dissolved in N-methylpyrrolidone (190 ml), and the mixture was stirred under ice-cooling. Then, 60% sodium hydride (2.08 g, 52 mmol) was added, and the mixture was stirred at the same temperature for 40 min. Then, ethyl iodide (3.3 ml, 53 mmol) was added, and the mixture was stirred at the same temperature for 2 hr. To the reaction mixture was added diluted aqueous sodium hydroxide solution, and the mixture was extracted with an ethyl acetate-hexane=1:1 mixed solvent. The organic layer was washed with diluted aqueous sodium hydroxide solution, water and saturated brine, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the solution was concentrated under reduced pressure. The obtained oil was purified by silica gel column chromatography (ethyl acetate-hexane), and the obtained solid was washed with hexane and dried under reduced pressure to give the title compound (4.53 g, yield 52%) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513235B2
Source datasetuspto-grants-2013_08
ORD IDord-5c590797463b489881f00ba923278708
Source noteuspto-grants-2013_08