HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131339Erstellt: 24. Oktober 2026
2,5-Dichloronitrobenzene → 2-(4-Chloro-2-nitro-phenylamino)-5-isopropyl-benzonitrile
https://huagongshe.com/de/reaction/131339
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Amino-5-isopropylbenzonitrile | HCID 21093463 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(4-Chloro-2-nitro-phenylamino)-5-isopropyl-benzonitrile | HCID 58625913 | 37,5% |
Reaktionsschritte
Combine 1,4-dichloro-2-nitro-benzene (0.513 g, 2.67 mmol), 2-amino-5-isopropyl-benzonitrile (0.514 g, 3.21 mmol), potassium carbonate (0.754 g, 5.45 mmol), and fine granular copper (0.031 g, 0.48 mmol) in dimethylformamide (5 ml). Heat the reaction mixture to 160° C. for 16 hours, and cool to ambient temperature. Dilute the reaction mixture with 50 ml of ethyl acetate and wash 3 times with 50 ml water and once with 50 ml of brine. Collect organic layer, dry over sodium sulfate and evaporate solvent. Purify the residue via flash chromatography eluting with a step gradient starting with 90% hexanes: 10% ethyl acetate and going to 85% hexanes: 15% ethyl acetate to obtain 0.316 g (1.00 mmol, 37% yield) of the title compound as an orange amorphous solid: Mass Spectrum (m/e): 316 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07384934B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-a83dd514648e44d0b7a77a4865d5711b |
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| Quellennotiz | uspto-grants-2008_06 |
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