Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Silicon carbide | HCID 9863 | — |
| Edukt | 2-(1,1-Dimethylethyl)-3-phenyloxaziridine | HCID 98371 | — |
| Produkt | N-tert-Butyl-a-phenylnitrone | HCID 4390 | — |
Reaktionsschritte
To a nitrogen charged 250 ml, 3-necked, round bottom flask equipped with a magnetic stir bar, nitrogen gas flow, pot thermometer, and condenser was added 119.3 gm (0.674 moles) of the 2-t-butyl-3-phenyloxaziridine as prepared in Example 2 and several silicon carbide boiling chips. The system was continuously flushed with nitrogen while gradually heated to 120° C. Upon reaching 120°, the heat was removed as the exothermic rearrangement brought the reaction temperature to about 134° C. before slowly subsiding. The pale yellow 2-t-butyl-3-phenyloxaziridine gradually turned to a clear, dark brown color. The reaction was cooled after a total reaction time of about 1 hour and a GC analysis, as described in Example 1, of the crude product 25 indicated a complete conversion to the corresponding nitrone (a peak having a retention time of 6.45 minutes). Upon cooling, the liquid N-t-butylphenylnitrone crystallized to form a solid having a crude yield of 109.4 gm (91.7% of theoretical yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06762322B1 |
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| Quelldatensatz | uspto-grants-2004_07 |
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| ORD ID | ord-6eb2d8e176a54055b37f743912b3aa15 |
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| Quellennotiz | uspto-grants-2004_07 |
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