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 solution of 2-{(RS)-1-[(3SR,4RS)-1-benzyl-4-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethoxy}-5-chloro-pyridine (XIV-B-2) 1.57 g (3.40 mmol) dissolved in CH3CN (40 mL) was added 1.08 mL (5.10 mmol) of 2,2,2-trichloroethyl chloroformate and stirring was continued for 3 hours at RT. Volatiles were removed under vacuo, and the residue was dissolved in AcOH (30 mL) before a total of 1.20 g of Zn dust was added portion wise. After three hours at RT, the reaction mixture was filtered on celite, the solvent removed under vacuo, followed by an extraction with EtOAc/aq. NaHCO3 (basic pH). The organic phases were dried on Na2SO4 and column chromatography (SiO2, CH2Cl2/MeOH 9:1) yielded 0.54 g (67%) of the title compound as a colorless oil. ES-MS m/e: 356.3 (M+H+).
WORKUP
后处理
- customVolatiles were removed under vacuo
- dissolutionthe residue was dissolved in AcOH (30 mL) before a total of 1.20 g of Zn dust
- additionwas added portion wise
- waitAfter three hours at RT
- filtrationthe reaction mixture was filtered on celite
- customthe solvent removed under vacuo
- extractionfollowed by an extraction with EtOAc/aq
- dry with materialThe organic phases were dried on Na2SO4 and column chromatography (SiO2, CH2Cl2/MeOH 9:1)