HRID502072
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
PROCEDURE
实验过程
To a mixture of enantiomer 1 of 4-{1-ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl-phenyl]-propyl}-N-methoxy-2,N-dimethyl-benzamide (1.0 g, 2.42 mmol) and THF (10 mL) is added 1M in THF LAH (2.5 mL, 2.55 mmol) with cooling. THF (5 mL) was added and the solution stirred for 1 hour. The solution is diluted with Et2O (100 mL) and washed with 1M HCl (50 mL). The aqueous phase is extracted with Et2O (50 mL). The combined organic layers are washed with 1M HCl (50 mL), brine (50 mL), dried over MgSO4, filtered and concentrated to furnish the title compound (0.64 g, 1.61 mmol, 67%).
WORKUP
后处理
- temperaturewith cooling
- washwashed with 1M HCl (50 mL)
- extractionThe aqueous phase is extracted with Et2O (50 mL)
- washThe combined organic layers are washed with 1M HCl (50 mL), brine (50 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated