HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethyl Acetate → 2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 4,5-Difluoro-2-nitroaniline | HCID 157151 | — |
| Edukt | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Edukt | 2-Fluoro-5-(trifluoromethyl)benzonitrile | HCID 521016 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Produkt | 2-(4,5-Difluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile | HCID 58625964 | 50,5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07384934B2 |
| Quelldatensatz | uspto-grants-2008_06 |
| ORD ID | ord-9f2ac96a8a4a4b6999fcc549bb9bedd3 |
| Quellennotiz | uspto-grants-2008_06 |