Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Levodopa | HCID 6047 | — |
| Edukt | Acetyl chloride | HCID 6367 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Melevodopa | HCID 23497 | 117,3% |
Reaktionsschritte
A 3-Liter three-necked round-bottom flask equipped with a cooling bath, a thermometer and a condenser was charged with 1.5 Liters methanol, and acetyl chloride (119 ml, 1.2 mol) was carefully added thereto at 0° C. The cooling bath was replaced with a heating mantle and the mixture was heated to 15° C. 60 grams (0.3 mol) of L-3-(3,4-dihydroxy-phenyl)alanine was then added and the reaction mixture was refluxed for 3 hours and thereafter concentrated under reduced pressure at 60° C. to afford 74.3 grams (100% yield) of Compound 2 (see, Scheme 1). The product structure was confirmed by 1H-NMR.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08207369B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-4a47b9208e444a0f9d11a7aa6fff6a61 |
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| Quellennotiz | uspto-grants-2012_06 |
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