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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286442Generated: October 27, 2026

4-(Trifluoromethyl)aniline → alpha-cyano-beta-(4-trifluoromethylanilino)-N-ethoxycarbonylacrylamide

https://huagongshe.com/reaction/2286442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactantethyl N-(2-cyano-3-ethoxyacryloyl)carbamateHCID 230015—
SolventEthanolHCID 702—
Productalpha-cyano-beta-(4-trifluoromethylanilino)-N-ethoxycarbonylacrylamideHCID 7054686590.8%

Reaction Steps

A mixture of α-cyano-β-ethoxy-N-ethoxycarbonylacrylamide (10 g) and 45 ml of ethanol is heated to effect dissolution. Then 8.12 g of p-trifluoromethylaniline in 10 ml of ethanol is added and the mixture heated at reflux for 45 minutes. The mixture is cooled and filtered to give 14.01 g of α-cyano-β-(4-trifluoromethylanilino)-N-ethoxycarbonylacrylamide, which is added to about 60 ml of tetralin and heated at reflux for several hours. On formation of precipitate, the mixture is allowed to cool and then filtered, washed with ether, to yield 5-cyano-1-(4-trifluoromethylphenyl)uracil, m.p. 230.5°-231.5°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04266056
Source datasetuspto-grants-1981_05
ORD IDord-cfb42bb3ec374da0abf711957583dc82
Source noteuspto-grants-1981_05