Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088838Generated: November 3, 2026

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

https://huagongshe.com/reaction/2088838

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 numberUS08436006B2
Source datasetuspto-grants-2013_05
ORD IDord-b9850a6552754ec2a3566a5d283ef11b
Source noteuspto-grants-2013_05