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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390272Generated: October 25, 2026

Ethanol → 3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrile

https://huagongshe.com/reaction/390272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant3-CyanophenolHCID 13394—
Reactant5-Fluoro-2-nitrobenzaldehydeHCID 587090—
Product3-(3-Dimethoxymethyl-4-nitrophenoxy)-benzonitrileHCID 58625053—

Reaction Steps

A mixture of 3-cyanophenol (0.38 mol) in ethanol (600 mL) was stirred at room temperature and K2CO3 (0.29 mol) was added. 5-fluoro-2-nitrobenzaldehyde (0.18 mol) was added, and the reaction mixture was stirred and refluxed for 4 hours. The solvent was evaporated, and the residue was stirred in water and extracted with CH2Cl2. The organic layer was separated, dried, filtered off and the solvent was evaporated. The residue was triturated under diisopropyl ether, and then the formed solids were filtered off and dried to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383637B2
Source datasetuspto-grants-2013_02
ORD IDord-1f2124a3aa644c6faf7e1b14e328c3a7
Source noteuspto-grants-2013_02