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
- 2.5 °C
PROCEDURE
实验过程
Taurine (1 g; 8 mmol) was dissolved in 2N NaOH (4.3 mL) and, after cooling on ice/water bath, 4N NaOH (2.14 mL) and a solution of benzyloxycarbonyl chloride (3.27 mL; 8 mmol) in toluene (3 mL) were dropped at same time. After the additions, the mixture was left stirring at T=0-5° C. for 1 h. The reaction was quenched by adding diethyl ether. The mixture was debated and the phases were separated. The aqueous one was cooled to 0-5° C. and 37% HCl was added to pH=2. The acidic phase was extracted with ethyl acetate (3×10 mL) and the collected organic extracts were washed with water (2×15 mL) and brine (15 mL), dried over Na2SO4 and evaporated under vacuum to give 2-(N-benzyloxycarbonylamino)ethanesulfonic acid as crude product purified by trituration in diethyl ether to give the pure product as white solid (1.46 g; 5.64 mmol Yield=70.5%)
WORKUP
后处理
- temperatureafter cooling on ice/water bath
- waitAfter the additions, the mixture was left
- customThe reaction was quenched
- additionby adding diethyl ether
- customthe phases were separated
- temperatureThe aqueous one was cooled to 0-5° C.
- addition37% HCl was added to pH=2
- extractionThe acidic phase was extracted with ethyl acetate (3×10 mL)
- washthe collected organic extracts were washed with water (2×15 mL) and brine (15 mL)
- dry with materialdried over Na2SO4
- customevaporated under vacuum