HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzoyl Peroxide → 4-(Benzoxazol-2-yl)benzyl bromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 2-p-Tolylbenzoxazole | HCID 70039 | — |
| Lösungsmittel | Carbon Tetrachloride | HCID 5943 | — |
| Produkt | 4-(Benzoxazol-2-yl)benzyl bromide | HCID 11033515 | — |
Reaktionsschritte
A stirred solution of 20.9 g (0.1 mole) of 2-(4-methylphenyl)benzoxazole, 17.8 g (0.1 mole) of N-bromosuccinimide, and 0.4 g (0.2 mole %) of benzoyl peroxide in carbon tetrachloride is heated at reflux for 20 hours. After cooling to room temperature, the reaction is diluted by the addition of carbon tetrachloride, and the solid byproducts are removed by filtration. The filtrate is concentrated in vacuo, and the product is purified by recrystallization from benzene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05247042 |
| Quelldatensatz | uspto-grants-1993_09 |
| ORD ID | ord-5c4084f677714fefb5da04262b23b483 |
| Quellennotiz | uspto-grants-1993_09 |