HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Aniline → 2-Norbornylphenylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Aniline | HCID 6115 | — |
| Edukt | Bicyclo(2.2.1)heptan-2-one | HCID 10345 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | HCID 178418385 | HCID 178418385 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 2-Norbornylphenylamine | HCID 54125158 | 106,9% |
Reaktionsschritte
In a 250 mL flask equipped with a Dean-Start separator, the following mixture is brought to reflux: 9.3 g of aniline, 12.1 g 2-norbornanone, 13.2 g benzotriazole and 120 mL xylene. After 16 h, the mixture is reduced to dryness, then it is solubilized in 300 mL methanol, and the product is reduced with 6 g NaBH4 at 50° C. for 1 h. The mixture is then poured into 200 mL water and the organic product is extracted with 3×100 mL toluene. The organic phase is recovered, dried over magnesium sulfate, and then reduced to dryness. In this manner, 20 g of the desired amine are produced.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06030555 |
| Quelldatensatz | uspto-grants-2000_02 |
| ORD ID | ord-cae0fbda27d04fde94c95b484282019f |
| Quellennotiz | uspto-grants-2000_02 |