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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231425Generated: November 1, 2026

Diethyl Ether → N-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]acetamide

https://huagongshe.com/reaction/231425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium MethoxideHCID 10942334—
Reactant1-(2-Chloro-4-fluoro-5-methylcarbonylaminophenyl)ethyl nitrateHCID 14501807—
SolventMethanolHCID 887—
ProductN-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]acetamideHCID 14501808—

Reaction Steps

To a clear, colorless solution of 0.4 g (0.0015 mole) of 1-(2-chloro-4-fluoro-5-methylcarbonylaminophenyl)ethyl nitrate in 15 ml of absolute methanol was added dropwise 0.31 g (0.0015 mole) of a 25 weight percent solution of sodium methoxide in methanol. The reaction mixture turned pale yellow immediately and was stirred at room temperature for 2.5 hours. An additional 0.31 g (0.0015 mole) of the sodium methoxide solution was added, and stirring at room temperature continued for 18 hours. The mixture was heated at reflux for 2.5 hours and then was allowed to cool to room temperature. To the mixture was added 100 ml of diethyl ether, and this mixture was washed with water. The diethyl ether solution was dried, filtered, and the solvent was evaporated under reduced pressure, yielding 0.28 g of N-[4-chloro-2-fluoro-5-(1-methoxyethyl)phenyl]acetamide. The nmr and ir spectra were consistent with the proposed structure. This reaction was repeated to provide sufficient starting material for Step G.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04846882
Source datasetuspto-grants-1989_07
ORD IDord-89a09a998bbf47828e7dbdc9e758b2a0
Source noteuspto-grants-1989_07