Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | p-Toluenesulfonyl azide | HCID 13661 | — |
| Edukt | 1,3-Cyclohexanedione, 5-phenyl- | HCID 568962 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1,3-Cyclohexanedione, 2-diazo-5-phenyl- | HCID 10889250 | 36,9% |
Reaktionsschritte
A solution of 20.0 g (0.106 mol) of 5-phenyl-cyclohexane-1, 3-dione in 75 ml ethanol was cooled to -10° C. and stirred magnetically under nitrogen. To the mixture was added 10.75 g (0.106 mol) of triethylamine. The tosyl azide (20.95 g 0.106 mol) was added all at once, and the mixture stirred for one hour at 0°-5° C. The solvent was removed under vacuum at a temperature less than 40° C. To the residue was added 200 ml ether, and the mixture extracted with a solution containing 3.1 g potassium hydroxide in 200 ml of water. The ethereal solution was dried over anhydrous MgSO4 filtered and the solvent removed to give a yellow solid which was recrystallized from ethanol-hexane to give 8.38 g (32%) of 2-diazo-5-phenyl-cyclohexane-1, 3-dione as yellow crystals, mp 122°-124° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04257858 |
|---|
| Quelldatensatz | uspto-grants-1981_03 |
|---|
| ORD ID | ord-af3b91f662af4a14b9cdb2db6487acfd |
|---|
| Quellennotiz | uspto-grants-1981_03 |
|---|