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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131335Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/131335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt4,5-Difluoro-2-nitroanilineHCID 157151—
EduktLithium hydroxide, monohydrateHCID 168937—
Edukt2-Fluoro-5-(trifluoromethyl)benzonitrileHCID 521016—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrileHCID 5862596450,5%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384934B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-9f2ac96a8a4a4b6999fcc549bb9bedd3
Quellennotizuspto-grants-2008_06