HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Toluene → N-[2-(1-cyclohexen-1-yl)-1-cyclohexen-1-yl]hexanamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Hexanamide | HCID 12332 | — |
| Edukt | Cyclohexenylcyclohexanone | HCID 101175 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-[2-(1-cyclohexen-1-yl)-1-cyclohexen-1-yl]hexanamide | HCID 21481520 | — |
Reaktionsschritte
2-(1-Cyclohexenyl)cyclohexanone (17.8 g., 0.1 mole), hexanamide (11.5 g., 0.1 mole), 5.0 g. of a highly acidic resin, Amberlyst 15, and toluene (150 ml) are mixed, stirred and heated at reflux for 16 hours. The water formed in the course of the reaction is azeotroped from the reaction mixture. The hot solution is decanted from the Amberlyst catalyst, the catalyst washed with toluene (200 ml.), and the toluene fractions are combined. Pentane (300 ml.) is added to the toluene solution, the mixture chilled in ice and filtered to remove 3.65 g. of unreacted hexanamide. The orange filtrate is stripped to yield 24 g. of crude product, an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04006236 |
| Quelldatensatz | uspto-grants-1977_02 |
| ORD ID | ord-f96a01e1938a476f950aff32e9e0c337 |
| Quellennotiz | uspto-grants-1977_02 |