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
- -15 °C
PROCEDURE
实验过程
To a solution of (R)-tert-butyl 3-(3-chlorobenzoyl)piperidine-1-carboxylate (92 g, 0.286 mol) in anhydrous THF (300 mL) at −15° C. under nitrogen was added drop wise a solution of 1 M R-CBS-oxazaborolidine in toluene (45 mL, 45 mmol, 0.15 eq). After stirring for 1 hr at −15° C., a solution of 10 M BH3 in THF (33 mL, 0.33 mol, 1.1 eq) was added drop wise. After addition, the reaction mixture was stirred for 2 h at −15° C. TLC indicated the starting material was consumed. Methanol (200 mL) was added drop wise carefully at −15° C. The solvent was removed under reduced pressure, the residue was purified by column chromatography on silica gel eluting with AcOEt/hexane (1:30→1:15) to provide a light yellow oil (82 g, HPLC≧70%, ratio≧3:1). The mixture was dissolved in ethyl acetate until the alcohol was just dissolved (about 5 mL/1 g), the solvent was removed on the rotary evaporator until a few of crystals appeared. The solution was cooled to room temperature slowly and stood for 1-2 h. To the above solution was added hexane (about 300 mL) and then filtered, the crystals were washed with cool hexane and recrystallized another two times to afford (R)-tert-butyl 3-((R)-(3-chlorophenyl)(hydroxy)methyl)piperidine-1-carboxylate as the pure isomer (32.5 g, ee.≧99%, yield 35% for two steps).
WORKUP
后处理
- additionAfter addition
- stirringthe reaction mixture was stirred for 2 h at −15° C
- customwas consumed
- additionMethanol (200 mL) was added drop wise carefully at −15° C
- customThe solvent was removed under reduced pressure
- customthe residue was purified by column chromatography on silica gel eluting with AcOEt/hexane (1:30→1:15)
- customto provide a light yellow oil (82 g, HPLC≧70%, ratio≧3:1)
- dissolutionwas just dissolved (about 5 mL/1 g)
- customthe solvent was removed on the rotary evaporator until a few of crystals
- temperatureThe solution was cooled to room temperature slowly
- waitstood for 1-2 h
- additionTo the above solution was added hexane (about 300 mL)
- filtrationfiltered
- washthe crystals were washed with cool hexane
- customrecrystallized another two times