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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848698Generated: October 30, 2026

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

https://huagongshe.com/reaction/848698

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 numberUS04297297
Source datasetuspto-grants-1981_10
ORD IDord-87ec9cf3b80f4dda893b00e06c9fd81d
Source noteuspto-grants-1981_10