Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2-Dimethoxyethane | HCID 8071 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Benzaldehyde, 4-(diphenylamino)- | HCID 77846 | — |
| Edukt | Trimethylphosphonium bromide | HCID 22062633 | — |
| Produkt | Vinyltriphenylamine | HCID 22283755 | 84% |
Reaktionsschritte
Into a three-necked flask, 14.6 g of sodium hydride and 700 ml of 1,2-dimethoxyethane were placed, and 130.8 g of trimethylphosphonium bromide was added thereto with stirring at room temperature. Next, after a drop of absolute alcohol was added, the reaction was allowed to proceed at 70° C. for 4 hours. Then, 100 g of 4-(N,N-diphenylamino)benzaldehyde was added thereto, and the temperature was raised to 70° C. to carry out reaction for 5 hours. The resulting reaction solution was filtered, and the filtrate and an ether-extract of the precipitate were put together and washed with water. Then, the ether solution was dehydrated with calcium chloride, and ether was removed to obtain a crude reaction product. After recrystallized from ethanol, acicular pale yellow vinyltriphenylamine was obtained in an amount of 83.4 g (yield: 84.0%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06296978B1 |
|---|
| Quelldatensatz | uspto-grants-2001_10 |
|---|
| ORD ID | ord-23407fedf46f4c59937f6c2c69f9ded1 |
|---|
| Quellennotiz | uspto-grants-2001_10 |
|---|