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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387695Generated: October 25, 2026

3-Fluoro-4-nitrophenol → 6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinoline

https://huagongshe.com/reaction/387695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Fluoro-4-nitrophenolHCID 520948—
Reactant4-Chloro-6-cyano-7-(2-methoxyethoxy)quinolineHCID 22646522—
SolventChlorobenzeneHCID 7964—
Product6-Cyano-4-(3-fluoro-4-nitrophenoxy)-7-(2-methoxyethoxy)quinolineHCID 2293657362.5%

Reaction Steps

4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (1.7 g) and 3-fluoro-4-nitrophenol (2.0 g) were suspended in chlorobenzene (20 ml), and the suspension was heated to reflux for 6 hours. After completion of the reaction, the solvent was distilled off, ethyl acetate was added, and a solid precipitated. The solid was filtered out and washed with ether, washed with 1N sodium hydroxide water and with water, and then dried to obtain 1.55 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-e45c9bc7abb24bbd8e51f63f71fd3892
Source noteuspto-grants-2013_02