反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -78 °C
PROCEDURE
实验过程
2 mmole (1 N 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 286 mg of pure (-)-galanthamine (a yield of 99.5%). HPLC of the resultant mixture indicates there is no epigalanthamine or lycoramine present. {m.p. 128°-129° C.; [α]D25 =-93.4}. Natural (-)-galanthamine has a melting point of 126°-127° C. ([α]D25 =-91.0)
WORKUP
后处理
- additionAfter addition
- temperaturewarmed to 0° C
- temperaturethe solution is warmed to 25° C.
- stirringstirred for 15 minutes
- customSolvent is then evaporated under vacuum to dryness
- customto obtain a syrup
- washThe column is eluted with a solvent mixture of CH2Cl2 /CH3OH 6:1