Reaktion #50740
ord-776d92d9740843baac2ed5cc2f7eae00
Reaktionsgleichung
L-Selectride
lithium tri-sec-butylborohydride
methanol
(+)-narwedine
→
(+)-galanthamine
Reagenzien
Keine
Reaktionsbedingungen
Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1workup.ADDITIONAfter addition
- 2Temperaturwarmed to 0° C
- 3Temperaturthe solution is warmed to 25° C.
- 4workup.STIRRINGstirred for 15 minutes
- 5SonstigeSolvent is then evaporated under vacuum to dryness
- 6Sonstigeto obtain a syrup
- 7WaschenThe column is eluted with a solvent mixture of CH2Cl2 /CH3OH 6:1
Vorschrift
2 mmole (1N in tetrahydrofuran {THF}) of L-Selectride® (lithium tri-sec-butylborohydride, Aldrich) is charged into 8 ml THF and cooled to -78° C. 1 mmole of (+)-narwedine in 50 ml THF is added dropwise over a period of 30 minutes. After addition, the solution is stirred at -78° C. for 2 hours and then warmed to 0° C. 0.4 ml of methanol is added and the solution is warmed to 25° C. and stirred for 15 minutes. Solvent is then evaporated under vacuum to dryness to obtain a syrup. The syrup is dissolved in 0.5 ml CHCl3 and the solution is loaded into a SiO2 200-400 mesh, 6A, column. The column is eluted with a solvent mixture of CH2Cl2 /CH3OH 6:1 to obtain pure (+)-galanthamine.