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-phenylcyclohexane-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 C-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-phenylcyclohexane-1,3-dione as yellow crystals, mp 122°-124° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04175135 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-7782474750034c419a283d1f22902368 |
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| Quellennotiz | uspto-grants-1979_11 |
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