Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660165Generated: October 27, 2026

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

https://huagongshe.com/reaction/1660165

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 affect 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 numberUS04307098
Source datasetuspto-grants-1981_12
ORD IDord-4c325c98e5014413ad9e13b724899761
Source noteuspto-grants-1981_12