Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:16])[C@@H:5]([O:14][CH3:15])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)[CH3:2].C(=O)([O-])[O-].[K+].[K+].S([O-])([O-])(=O)=O.[Mg+2].[CH2:29](Br)[CH2:30][Br:31]>CCO>[CH2:1]([O:3][C:4](=[O:16])[C@@H:5]([O:14][CH3:15])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([O:13][CH2:29][CH2:30][Br:31])=[CH:11][CH:12]=1)[CH3:2]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture containing (2S)-3-(4-hydroxy-phenyl)-2-methoxy-propionic acid ethyl ester obtained in Step 1 (0.223 mol, 50 mg), potassium carbonate (0.446 mol, 50 mg), magnesium sulfate (powdered, 50 mg, 1 g/g), ethylene dibromide (3.35 mol. 628 mg) and EtOH (25 mL) was heated at reflux (78–76° C.) for 24 hours and cool to room temperature. The mixture was heated again to reflux (76.5–77° C.) and 2 mL of ethylene dibromide was added. The mixture was heated for another 12 hours at 79.5–80.1° C. and then cooled to room temperature and vacuum filtered. The filtrate was concentrated under vacuum, and the residue was purified by column chromatography (silica gel, hexanes/ethyl acetate 6:1, Rf 027) to produce a colorless oil. MS (ES) for C14H19BrO4 [M+Na]+: 353.0.
Aufarbeitung
- temperaturewas heated
- temperatureat reflux (78–76° C.) for 24 hours
- temperatureThe mixture was heated again
- additionwas added
- temperatureThe mixture was heated for another 12 hours at 79.5–80.1° C.
- temperaturecooled to room temperature
- filtrationvacuum filtered
- concentrationThe filtrate was concentrated under vacuum
- customthe residue was purified by column chromatography (silica gel, hexanes/ethyl acetate 6:1, Rf 027)
- customto produce a colorless oil
Quellen und Nachweise
- ORD-Eintrag
- ord-9bdce17b3f9745cbabd0c9c4b53ffb28
- Quelldatensatz
- uspto-grants-2007_03
- Patentnummer
- US07192982B2
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