Reaktionsgleichung
S(Cl)(Cl)=O.[OH:5][C@H:6]1[CH2:10][NH:9][C@H:8]([C:11]([OH:13])=[O:12])[CH2:7]1.[CH3:14]O>>[OH:5][C@H:6]1[CH2:10][NH:9][C@H:8]([C:11]([O:13][CH3:14])=[O:12])[CH2:7]1Komponenten
4
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Thionyl chloride (270 mL) was added dropwise to methanol (1500 mL) over 1 hour, followed by the addition of (4R)-4-hydroxy-L-proline (150 g). The mixture was stirred at reflux for 36 hours, and then concentrated under reduced pressure. Methanol (1500 mL) was added, followed by a slow addition of triethylamine (310 mL). The mixture was cooled to 0° C., filtered, and the filtrate was concentrated to afford methyl (4R)-4-hydroxy-L-prolinate. The residue was used directly without further purification.
Aufarbeitung
- temperatureat reflux for 36 hours
- concentrationconcentrated under reduced pressure
- additionMethanol (1500 mL) was added
- additionfollowed by a slow addition of triethylamine (310 mL)
- filtrationfiltered
- concentrationthe filtrate was concentrated
Quellen und Nachweise
- ORD-Eintrag
- ord-ccbf0d3c4d19427fb2fc341df38aed51
- Quelldatensatz
- uspto-grants-2014_09
- Patentnummer
- US08846657B2
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