Reaktionsgleichung
C([O:4][C@H:5]([CH2:10]Br)[CH2:6][C:7]([OH:9])=[O:8])(=O)C.[CH:12]([NH:15][CH:16]([CH3:18])[CH3:17])([CH3:14])[CH3:13]>O>[CH:12]([NH:15][CH:16]([CH3:18])[CH3:17])([CH3:14])[CH3:13].[O:4]1[CH2:10][C@@H:5]1[CH2:6][C:7]([OH:9])=[O:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a 2 l of three-necked flask equipped with thermometer pH meter and mechanical stirrer were charged distilled water (1 l), (S)-3-acetoxy-4-bromobutyric acid (90 g, 0.4 mol) and diisopropylamine (121 g, 1.2 mol). The reaction mixture was stirred at 0˜5° C. for 2 hours to afford (S)-3,4-epoxybutyric acid diisopropylamine salt. Over 99% of conversion was detected by NMR.
Aufarbeitung
- customTo a 2 l of three-necked flask equipped with thermometer pH meter and mechanical stirrer
- additionwere charged
Quellen und Nachweise
- ORD-Eintrag
- ord-2155bc355ba64fc283209720a9a2af7e
- Quelldatensatz
- uspto-grants-2003_07
- Patentnummer
- US06586616B1
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