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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259907Generated: October 31, 2026

Sodium hydride → 5-fluoro-N-(4-methoxybutyl)-2-nitroaniline

https://huagongshe.com/reaction/1259907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Fluoro-2-nitroanilineHCID 75399—
Reactant4-Methoxybutyl methanesulfonateHCID 11687006—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product5-fluoro-N-(4-methoxybutyl)-2-nitroanilineHCID 5835575531.8%

Reaction Steps

5-Fluoro-2-nitroaniline (1.0 g) was dissolved in THF (20 ml), sodium hydride (60% in oil, 384 mg) was added, and the mixture was stirred at room temperature for 30 min. 4-Methoxybutyl methanesulfonate (1.28 g) was added, and the mixture was heated under reflux with stirring for 15 hr. The reaction mixture was cooled to room temperature and saturated brine was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (30:70) was concentrated under reduced pressure to give the object product (494 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466282B2
Source datasetuspto-grants-2013_06
ORD IDord-ce56c47c066542ae9e8a4b2b4621dcc9
Source noteuspto-grants-2013_06