HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1954Erstellt: 24. Oktober 2026
Dimethylformamide → 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene
https://huagongshe.com/de/reaction/1954
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 5-[N-(4-tolyl)-N-phenylamino]acenaphthene | HCID 19688913 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene | HCID 19688918 | 97,1% |
Reaktionsschritte
4.7 g (0.014 mol) of the above prepared 5-[N-(4-tolyl)-N-phenylamino]acenaphthene was dissolved in 30 ml of N,N-dimethylformamide, and 3.22 g (0.021 mol) of phosphorus oxychloride was dropwise added thereto at room temperature for 10 minutes. After the temperature was raised to 50° C., and the mixture was stirred for 14 hours. The reaction was determined to be finished when disappearance of 5-[N-(4-tolyl)-N-phenylamino]acenaphthene was identified. The reaction product was poured into an aqueous solution having 10 g (0.23 mol) of 93% sodium hydroxide dissolved in 250 ml of water. The resultant mixture was cooled to precipitate a crystal, which was then filtrated, washed with water and dried to obtain 4.94 g (yield: 97.1%) of 5-[N-(4-formylphenyl)-N-(4-tolyl)amino]acenaphthene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05728500 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-20078ac392344345839361b7b292e056 |
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| Quellennotiz | uspto-grants-1998_03 |
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