Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2-(Pyrid-3-yl)cyclohexanone | HCID 10976010 | — |
| Edukt | Di-t-butyl diazodicarboxylate | HCID 19106893 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Produkt | HCID 19106897 | HCID 19106897 | — |
Reaktionsschritte
Potassium t-butoxide (3.7 g, 33 mmol) was added, in one portion, to a stirred solution of 2-(pyrid-3-yl)cyclohexanone (5.3 g, 30 mmol) in dimethylformamide (60 ml) at 0° C. After 60 minutes the dark red solution was treated with di-t-butyl diazodicarboxylate (7.6 g, 33 mmol) over 5 minutes. The mixture was then allowed to warm to 20° C. over 1 hour, poured into saturated ammonium chloride solution (50 ml) and extracted with ethyl acetate (2×25 ml). The combined organic extracts were successively washed with water (20 ml) and saturated brine (20 ml) and dried over sodium sulphate. Concentration in vacuo gave the crude product which was recrystallised from petroleum ether (60°-80° C.; 150 ml) to give 2-(N,N'-di-t-butoxycarbonylhydrazino)-2-(pyrid-3-yl)cyclohexanone (7.1 g, 17.5 mmol), m.p. 123°-125° C.;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05276046 |
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| Quelldatensatz | uspto-grants-1994_01 |
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| ORD ID | ord-78a762870ee1455c8af616941c81c009 |
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| Quellennotiz | uspto-grants-1994_01 |
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