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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131335Generated: October 25, 2026

Ethyl Acetate → 2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile

https://huagongshe.com/reaction/131335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4,5-Difluoro-2-nitroanilineHCID 157151—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2-Fluoro-5-(trifluoromethyl)benzonitrileHCID 521016—
SolventDimethyl SulfoxideHCID 679—
Product2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrileHCID 5862596450.5%

Reaction Steps

Heat a solution of 2-fluoro-5-trifluoromethyl-benzonitrile (1.0 g, 5.74 mmol) with 4,5-difluoro-2-nitro-phenylamine (1.09 g, 5.74 mmol) and lithium hydroxide monohydrate (0.48 g, 11.49 mmol) in DMSO (12 ml) to 55° C. for 16 hours. Cool the reaction to ambient temperature and then add approximately 150 ml of ice water and stir the mixture for one hour. Extract with three 200 ml portions of dichloromethane. Combine organic layers, dry over sodium sulfate and evaporate solvent. Purify the residue via flash chromatography eluting with a linear gradient starting with 100% hexanes and going to 70% hexanes: 30% ethyl acetate to obtain 0.995 g (2.90 mmol, 50% yield) of the title compound as a yellow amorphous solid: Mass Spectrum (m/e): 344 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07384934B2
Source datasetuspto-grants-2008_06
ORD IDord-9f2ac96a8a4a4b6999fcc549bb9bedd3
Source noteuspto-grants-2008_06