Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | 3-Hydroxybutyrolactone, (3S)- | HCID 7269389 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (3S)-3-acetyloxy-4-bromobutanoic acid | HCID 2733880 | 95% |
Reaktionsschritte
To a 2 l of three-necked flask equipped with reflux condenser, thermometer and mechanical stirrer were charged (S)-3-hydroxy-γ-butyrolactone (102 g) and 30% of hydrobromic acid in acetic acid (675 g, 2.5 eq.). The mixture was stirred at 40° C. for 3 hours. After cooling the reaction mixture, methylene chloride (1000 ml) was added to it. The reaction mixture was washed with aqueous solution of sodium acetate. The organic layer was separated, dried over magnesium sulfate, and concentrated to afford (S)-3-acetoxy-4-bromobutyric acid (213 g, 95%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06586616B1 |
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| Quelldatensatz | uspto-grants-2003_07 |
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| ORD ID | ord-811ace35f479451696a4894ed030bdba |
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| Quellennotiz | uspto-grants-2003_07 |
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