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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758943Generated: October 27, 2026

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

https://huagongshe.com/reaction/1758943

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 numberUS04338318
Source datasetuspto-grants-1982_07
ORD IDord-5ea4a6dd84764541b837ed6c033c85ae
Source noteuspto-grants-1982_07