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
- 80 °C
PROCEDURE
实验过程
The mixture of 0.800 g of tert-butyl 3-(2-bromo-4-methylbenzyloxy)-4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}piperidine-1-carboxylate, 0.250 ml of benzophenone imine, 0.0037 g of dipalladiumtris(dibenzylidenacetone)-chloroform complex, 0.0051 g of (R)-(+)-2,2′-bis(diphenylphosphine)-1,1′-binaphthyl and 0.168 g of sodium tert-butoxide is admixed with 6.0 ml of toluene and stirred under argon at 80° C. over 72 hours. The reaction mixture is cooled, admixed with brine (20 ml) and extracted with ethyl acetate (2×80 ml). The organic phases are dried over sodium sulphate, filtered and concentrated by evaporation. The residue is dissolved in 6.0 ml of methanol, admixed with 0.090 g of 5% Pd/C and 1.15 g of ammonium formate, and stirred at 60° C. over 72 hours. The reaction mixture is diluted with methanol (20 ml) and clarified by filtration, and the filtrate is concentrated by evaporation. The residue is admixed with 0.1M NaOH (100 ml) and extracted with ethyl acetate (2×100 ml). The organic phases are washed successively with 0.1M NaOH (100 ml) and brine (100 ml), dried over sodium sulphate, filtered and concentrated by evaporation. The title compound is obtained as a yellowish oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.30 (1:2 EtOAc-heptane); Rt=5.32.
WORKUP
后处理
- temperatureThe reaction mixture is cooled
- extractionextracted with ethyl acetate (2×80 ml)
- dry with materialThe organic phases are dried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated by evaporation
- dissolutionThe residue is dissolved in 6.0 ml of methanol
- stirringstirred at 60° C. over 72 hours
- additionThe reaction mixture is diluted with methanol (20 ml)
- filtrationclarified by filtration
- concentrationthe filtrate is concentrated by evaporation
- extractionextracted with ethyl acetate (2×100 ml)
- washThe organic phases are washed successively with 0.1M NaOH (100 ml) and brine (100 ml)
- dry with materialdried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated by evaporation