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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982665Generated: October 30, 2026

4-Amino-2-(trifluoromethyl)benzonitrile → HCID 11246104, compound

https://huagongshe.com/reaction/982665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-(trifluoromethyl)benzonitrileHCID 522170—
Reactant3-(5-Chloropentyl)-4-methyl-2,5-furandioneHCID 11378943—
SolventEthanolHCID 702—
ProductHCID 11246104HCID 11246104—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 9.46 g of 3-(5-chloropentyl)-4-methyl-2,5-furandione and 8.13 g of 4-amino-2-(trifluoromethyl)benzonitrile in 22 ml of ethanol was mixed under a nitrogen atmosphere with 2.5 g of an activated molecular sieve (0.3 nm), and it was stirred for 2 days at 90° C. For working-up, the molecular sieve was filtered off after cooling, washed with ethanol, and the combined ethanol solutions were concentrated by evaporation. The residue was taken up in ethyl acetate and washed with water as well as saturated sodium chloride solution. After drying on sodium sulfate and concentration by evaporation, it was chromatographed on silica gel with ethyl acetate/hexane/toluene, and 11.69 g of the title compound was thus obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861432B2
Source datasetuspto-grants-2005_03
ORD IDord-4a049e2a72a5434eb0e8de77a4fe005e
Source noteuspto-grants-2005_03