HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzonitrile → Benzamide, N-1-adamantyl-
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzonitrile | HCID 7505 | — |
| Edukt | Adamantane | HCID 9238 | — |
| Edukt | N-Hydroxyphthalimide | HCID 10665 | — |
| Edukt | oxygen O2 | HCID 131723558 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | Benzamide, N-1-adamantyl- | HCID 29392 | 65% |
| Produkt | 1-Adamantanol | HCID 64152 | 7% |
| Produkt | 1-Nitroadamantane | HCID 64165 | 6% |
| Produkt | 1-Adamantyl acetate | HCID 519973 | 2% |
Reaktionsschritte
Into a flask, 1 mmole of adamantane, 0.1 mmole of N-hydroxyphthalimide, 6 ml of benzonitrile and 1 ml of acetic acid were added to mix and the flask was equipped with a gas bag (about 1L) of nitrogen monoxide NO. The mixture was reacted for 20 hours at 100° C. with stirring. The reaction products were analyzed by gas chromatography, and, as a result, the conversion of adamantane was 92%, and 1-benzoylaminoadamantane (yield 65%), 1-adamantanol (yield 7%), 1-nitroadamantane (yield 6%), 1-acetyloxyadamantane (yield 2%) and 2-adamantanone (yield 2%) were formed.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06468487B1 |
| Quelldatensatz | uspto-grants-2002_10 |
| ORD ID | ord-dbd02d744dfb40f88857f67c57f33a61 |
| Quellennotiz | uspto-grants-2002_10 |