Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | L-Homoserine | HCID 12647 | — |
| Edukt | 2-Dimethylaminopyridine | HCID 21885 | — |
| Produkt | N-(2-oxooxolan-3-yl)acetamide | HCID 325257 | 60% |
Reaktionsschritte
L-Homoserine (2 mol) was suspended in 900 ml of acetic anhydride and admixed with a spatula tip full of dimethylaminopyridine (DMAP). It was slowly heated to 60° C. After approximately 1 hour, the temperature rapidly increased to 100° C. Subsequently the reaction mixture was stirred at 80° C. for 90 minutes and concentrated to dryness under vacuum. The resultant yellow oil was taken up in isopropanol (600 ml) and allowed to stand overnight at 0° C. The resultant crystals were filtered off, washed with cold isopropanol and dried under vacuum. The yield was 60% N-acetyl-2-amino-4-butyrolactone isolated, the purity 99% (according to HPLC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07368600B2 |
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| Quelldatensatz | uspto-grants-2008_05 |
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| ORD ID | ord-352eca809da94d408397cf48d8d36b0f |
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| Quellennotiz | uspto-grants-2008_05 |
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