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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419893Generated: November 3, 2026

Ethanol → 2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamide

https://huagongshe.com/reaction/2419893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionitrileHCID 13384298—
SolventWaterHCID 962—
Product2-(4-Chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamideHCID 13384299—

Reaction Steps

A mixture of 2-(4-chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionitrile (20 g.), potassium hydroxide (25 g.), ethanol (250 ml.) and water (250 ml.) is heated under reflux for 15 minutes. Most of the ethanol is evaporated in vacuo, and the residue is cooled until the precipitated oil solidifies. The solid is filtered off, and is recrystallised from a mixture of ether and light petroleum (b.p. 40°-60° C.) (charcoal) to give 2-(4-chlorobenzyloxy)-3,3,3-trifluoro-2-trifluoromethylpropionamide, m.p. 94°-95° C. (13.9 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107329
Source datasetuspto-grants-1978_08
ORD IDord-cd33c756f5a4412e87f2c93fb50451fe
Source noteuspto-grants-1978_08