HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 249207Erstellt: 24. Oktober 2026
Potassium Iodide → N,N'-Dibenzyl-N,N'-diphenyl-p-phenylenediamine
https://huagongshe.com/de/reaction/249207
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Iodide | HCID 4875 | — |
| Edukt | N,N'-Diphenyl-P-Phenylenediamine | HCID 6319 | — |
| Edukt | Benzyl Chloride | HCID 7503 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N,N'-Dibenzyl-N,N'-diphenyl-p-phenylenediamine | HCID 15701549 | — |
Reaktionsschritte
A solution of N,N'-diphenyl-p-phenylenediamine (26 g, 0.1 mol) in toluene (400 ml) is treated sequentially with powdered potassium hydroxide (19.3 g, 0.3 mol), potassium iodide (1.7 g, 0.01 mol) and tetrabutylammonium bromide (1.6 g, 0.005 mol). The resulting mixture is vigorously stirred while benzyl chloride (27.9 g, 0.22 mol) is added dropwise. The mixture is slowly warmed to 90° C. over a one-hour period and then held there for four hours. The mixture is allowed to cool and methylene chloride (100 ml) is added. The resulting mixture is filtered and concentrated to a solid that is washed with water and dried. The title compound is obtained in a yield of 24.8 g (56%) as a tan solid melting at 145°-150° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05213699 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-4fae3e4d95f6415aba754cbf9b74f918 |
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| Quellennotiz | uspto-grants-1993_05 |
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