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 room temperature, stirred mixture of (S)-3-(4-benzyloxy-phenyl)-2-[4-(4-phenyl-piperidin-1-yl)-benzenesulfonylamino]-propionic acid (0.033 g, 0.000058 mol) in thioanisole (0.34 mL) was added trifluoroacetic acid (1 mL), and the mixture was stirred for 18 hours. The reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried (Na2SO4) and rotary-evaporated under reduced pressure to remove volatiles. The resulting yellow solution was chromatographed on silica gel (5.5 g) eluting with dichloromethane (10×5 mL) followed by dichloromethane-methanol (14:1). Fractions containing product were rotary-evaporated. The residue was suspended in water and stirred to give the title compound as an off-white solid; yield 0.0079 g (28%), mp 108-110° C.
WORKUP
后处理
- stirringthe mixture was stirred for 18 hours
- extractionextracted with ethyl acetate
- dry with materialThe organic layer was dried (Na2SO4)
- customrotary-evaporated under reduced pressure
- customto remove volatiles
- customThe resulting yellow solution was chromatographed on silica gel (5.5 g)
- washeluting with dichloromethane (10×5 mL)
- additionFractions containing product
- customwere rotary-evaporated
- stirringstirred