Reaktion #50740

ord-776d92d9740843baac2ed5cc2f7eae00

Reaktionsgleichung

CCC(C)[BH-](C(C)CC)C(C)CC.[Li+]
L-Selectride
CCC(C)[BH-](C(C)CC)C(C)CC.[Li+]
lithium tri-sec-butylborohydride
CO
methanol
COc1ccc2c3c1O[C@@H]1CC(=O)C=C[C@]31CCN(C)C2
(+)-narwedine
COc1ccc2c3c1O[C@@H]1C[C@H](O)C=C[C@]31CCN(C)C2
(+)-galanthamine

Lösungsmittel

Reaktionsbedingungen

Temperatur
-78°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    Temperaturwarmed to 0° C
  3. 3
    Temperaturthe solution is warmed to 25° C.
  4. 4
    workup.STIRRINGstirred for 15 minutes
  5. 5
    SonstigeSolvent is then evaporated under vacuum to dryness
  6. 6
    Sonstigeto obtain a syrup
  7. 7
    WaschenThe 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05428159uspto-grants-1995_06