HRID239572
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
N2-{[(1,1-dimethylethyl)oxy]carbonyl}-2-methylalaninamide (3.87 g, 19.13 mmol), Lawesson's reagent (7.74 g, 19.13 mmol) and tetrahydrofuran (THF) (100 mL) was heated to 50° C. for 3 hours. The reaction was concentrated, added 150 cc of EtOAc and washed with sat'd NaHCO3 (3×100 cc), water and brine. The EtOAc layer was concentrated and the residue was purified via chromatography on silica gel eluted Hex to 1:1 Hex/EtOAc to obtain the title compound (2.04 g, 48% yield).
WORKUP
后处理
- concentrationThe reaction was concentrated
- additionadded 150 cc of EtOAc
- washwashed with sat'd NaHCO3 (3×100 cc), water and brine
- concentrationThe EtOAc layer was concentrated
- customthe residue was purified via chromatography on silica gel eluted Hex to 1:1 Hex/EtOAc