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
- 0 °C
PROCEDURE
实验过程
To a solution of Boc-L-serine (10.3 g, 50 mmol) in 75 mL of H2O:t-BuOH (2:1) is added methoxyamine hydrochloride (23 g, 75 mmol) and 1-(3-dimethyl-aminopropyl)-3-ethylcarbodiimide hydrochloride (9.6 g, 50 mmol). After 2 hours, the solution is saturated with NaCl. The solution is extracted with EtOAc. The organic layer is dried over MgSO4, filtered and concentrated. The resulting crude material is dissolved in 50 mL of pyridine and cooled to 0° C. To the solution is added methane sulfonyl chloride (7.44 g, 65 mmol). After 1 hour, the solution is poured into 100 mL of cold 1 N HCl (aq.). The solution is diluted with EtOAc. The layers are separated and the organic layer is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The resulting crude material is dissolved in 50 mL of acetone and added dropwise to a solution of K2CO3 (20.7 g, 150 mmol) in 900 mL of acetone at reflux. After 1 hour, the solution is cooled to ambient temperatures. The solution is filtered through Celite. The collected organic solution is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The resulting solid is dissolved in 20 mL of THF and added dropwise to an ammonia solution containing sodium (2.6 g, 113 mmol) at -78° C. After the blue color has dissipated, the solution is stirred for an additional 10 minutes. To the reaction mixture is added NH4Cl (13.4 g, 250 mmol) and the solution is allowed to warm to ambient temperatures. The solution is filtered. The collected solution is concentrated. The resulting residue is recrystallized from EtOAc to give the title compound (2 g, 11 mmol) as a white solid.
WORKUP
后处理
- extractionThe solution is extracted with EtOAc
- dry with materialThe organic layer is dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe resulting crude material is dissolved in 50 mL of pyridine
- waitAfter 1 hour
- customThe layers are separated
- washthe organic layer is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl
- dry with materialThe organic layer is dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe resulting crude material is dissolved in 50 mL of acetone
- temperatureat reflux
- waitAfter 1 hour
- temperaturethe solution is cooled to ambient temperatures
- filtrationThe solution is filtered through Celite
- washThe collected organic solution is washed with 1 N HCl, saturated NaHCO3 and saturated NaCl
- dry with materialThe organic layer is dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe resulting solid is dissolved in 20 mL of THF
- additionadded dropwise to an ammonia solution
- temperatureto warm to ambient temperatures
- filtrationThe solution is filtered
- concentrationThe collected solution is concentrated
- customThe resulting residue is recrystallized from EtOAc