Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Allyl isocyanate | HCID 15123 | — |
| Edukt | 3H-Pyrazol-3-one, 2,4-dihydro-5-methyl- | HCID 319771 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178457912 | HCID 178457912 | 51,1% |
Reaktionsschritte
Potassium carbonate (3.52 g, 25.5 mmol) was added to a solution of 3-hydroxy-5-methylpyrazole (5.00 g, 51.0 mmol) in DMF (80 ml). Then, allylisocyanate (4.51 ml, 51.0 mmol) was added, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid and extracted with ethyl acetate (50 ml×2). An organic layer was washed with water (50 ml×3), dried over anhydrous magnesium sulfate and then filtered to remove a desiccant, and the solvent was distilled off from a filtrate under reduced pressure. The resultant crude product was purified with a silica gel column (ethyl acetate/hexane=1/3), to give a white solid of N-allyl-3-hydroxy-5-methylpyrazole-1-carboxamide (4.72 g, yield: 51.1%). mp: 80-83° C.; 1H-NMR (CDCl3, TMS, ppm): δ 2.55 (d, J=0.8 Hz, 3H), 3.97 (dddt, J=1.6, 1.6, 5.8 and 5.8 Hz, 2H), 5.19 (ddt, J=1.6, 2.7 and 10.3 Hz, 1H), 5.28 (ddt, J=1.6, 2.7 and 17.2 Hz, 1H), 5.63 (d, J=0.8 Hz, 1H), 5.90 (ddt, J=5.8, 10.3 and 17.2 Hz, 1H), 6.70 (m, 1H). (Hydroxy proton was not assigned.)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07700786B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-c2403f4a42724180b1c8ace5380d6ebb |
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| Quellennotiz | uspto-grants-2010_04 |
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