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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086374Generated: October 31, 2026

4-(Trifluoromethyl)aniline → Leflunomide

https://huagongshe.com/reaction/2086374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactant5-Methyl-1,2-oxazole-4-carbonyl chlorideHCID 2759917—
SolventTolueneHCID 1140—
SolventDimethylacetamideHCID 31374—
SolventSodium BicarbonateHCID 516892—
ProductLeflunomideHCID 389986.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

4-Trifluoromethylaniline (5.75 g, 35.7 mm) was dissolved in a mixture of NaHCO3 (3.16 g, 37.6 mm), N,N-dimethylacetamide (0.7 ml, 7.5 mm) and toluene (70 ml). The mixture was warmed to 40° C. and 5-methylisoxazole-4-carboxylic acid chloride (5 g, 34.4 mm) was added dropwise over 20 min. The mixture was stirred at this temperature for another 3 h. and then it was heated to reflux temperature. The hot mixture was washed with water (3×10 ml). The organic phase was allowed to cool to ambient temperature, which induced leflunomide to precipitate as a white powder. The powder was isolated by filtration and then dried at 60° C. to give leflunomide (8.0 g, 86%) in 99.5% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06723855B2
Source datasetuspto-grants-2004_04
ORD IDord-cb0f6b5efcf3449cbd3b1a8808f4caef
Source noteuspto-grants-2004_04