Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Nicotinate | HCID 7151 | — |
| Edukt | 1-(But-1-enyl)pyrrolidin-2-one | HCID 580170 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Myosmine | HCID 442649 | 77,2% |
Reaktionsschritte
Sodium hydride (17.26 g, 072 mol of 60% dispersion in a mineral oil) was washed with toluene (25 ml×2) to remove mineral oil and added to 25 ml of DMF. To this a solution containing 1-(but-1-enyl)-pyrrolidin-2-one (I, 50 g, 0.3597 mol) and methyl nicotinate (41.8 g, 0.3057 mol) in 50 ml of DMF was added. The reaction mixture was heated to 90° C. for 2 hrs. DMF was partially removed under reduced pressure and 100 ml water and HCl (165 ml) were added. The reaction mixture was heated to 110° C. for 12 hr, cooled and washed with ethyl acetate (50 ml×2). The aqueous layer was cooled to 0° C., pH adjusted to about 14 using NaOH, extracted with dichloromethane (100 ml×4), the extract dried over Na2SO4, the solvent removed completely and the crude solid was purified by high vacuum distillation to get myosmine (34.38 g, 77.2% yield, 98.5% purity by GC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367837B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-33517937e2044864ac997c57c365dae4 |
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| Quellennotiz | uspto-grants-2013_02 |
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