Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Cyanopyridine | HCID 7506 | — |
| Edukt | 4-(Methylsulfonyl)aniline hydrochloride | HCID 2735180 | — |
| Edukt | Trimethylaluminum | HCID 16682925 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | HCID 178504801 | HCID 178504801 | — |
Reaktionsschritte
To a suspension of 4-(methylsulfonyl)aniline hydrochloride (10 g, 48.1 mmol) in toluene (250 ml) at 0° C., trimethylaluminum (2M solution in toluene, 36.1 ml, 72.2 mmol) was added over 10 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 4-cyanopyridine (10 g, 96.2 mmol) in toluene (250 ml) was added over 10 minutes and the mixture was heated to 70° C. After 24 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the residue was washed with a mixture of methylene chloride/methanol and later with methanol. The combined filtrates were concentrated and the resulting yellowish solid was stirred with ethyl acetate and filtered. The pale yellow solid (4.8 g, 36%) was used in the next reaction without further purification. Anal. Calc'd. for C13H14N3SClO2H2O: C, 47.34, H, 4.89, N, 12.74, S, 9.72. Found: C, 47.69, H, 4.35, N, 12.77, S, 9.74.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05616601 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-4f242085bc2e4a4d9b904bc7ce25393b |
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| Quellennotiz | uspto-grants-1997_04 |
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