Sodium Methoxide → (2S,3R)-3-(4-benzyloxy-2-trifluoromethyl-phenyl)-2-ethoxy-3-hydroxy-propionic acid methyl ester
Reaktionsgleichung
C([C@H]1COC(=O)N1[C:14](=[O:39])[C@@H:15]([O:36][CH2:37][CH3:38])[C@@H:16]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[CH:20][C:19]=1[C:32]([F:35])([F:34])[F:33])[OH:17])C1C=CC=CC=1.[CH3:40][O-:41].[Na+]>CO>[CH3:40][O:41][C:14](=[O:39])[C@@H:15]([O:36][CH2:37][CH3:38])[C@@H:16]([C:18]1[CH:23]=[CH:22][C:21]([O:24][CH2:25][C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)=[CH:20][C:19]=1[C:32]([F:34])([F:35])[F:33])[OH:17]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In analogy to the procedure described in example 1 b], (S)-4-benzyl-3-[(2S,3R)-3-(4-benzyloxy-2-trifluoromethyl-phenyl)-2-ethoxy-3-hydroxy-propionyl]-oxazolidin-2-one was treated with sodium methoxide in methanol to give (2S,3R)-3-(4-benzyloxy-2-trifluoromethyl-phenyl)-2-ethoxy-3-hydroxy-propionic acid methyl ester as colorless liquid. According to 1H-NMR spectroscopy, one single diastereomer was obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-e4330b52d3cf48c3a38d131613af18a5
- Quelldatensatz
- uspto-grants-2005_11
- Patentnummer
- US06969725B2
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