反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
CONDITIONS
反应条件
- 温度
- -70 °C
PROCEDURE
实验过程
Sec butyllithium (298 ml: 1.3 M) was added dropwise at −60° C. under N2 flow to a solution of N-(4-bromophenyl)acetamide (0.1892 mol) in THF (400 ml) and the mixture was stirred at −70° C. for 2 hours. A solution of 1-cyano-1-methyl-N,N-dimethylethanamine (0.075 mol) in THF (60 ml) was added dropwise, the mixture was brought to RT and then stirred at RT for 12 hours. The mixture was poured into ice and extracted with EtOAc. The solvent was evaporated, the residue was taken up in HCl (3 N) and EtOAc, extracted with EtOAc, basified with K2CO3 (10%) and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was recrystallized from (C2H5)2O and DIPE. The precipitate was filtered off and dried, yielding 6.8 g (36%) of N-[4-[2-(dimethylamino)-2-methyl-1-oxopropyl]phenyl]acetamide (interm. 3).
WORKUP
后处理
- customwas brought to RT
- stirringstirred at RT for 12 hours
- additionThe mixture was poured into ice
- extractionextracted with EtOAc
- customThe solvent was evaporated
- extractionEtOAc, extracted with EtOAc
- extractionextracted with CH2Cl2
- customThe organic layer was separated
- customdried
- filtrationfiltered
- customthe solvent was evaporated
- customThe residue was recrystallized from (C2H5)2O and DIPE
- filtrationThe precipitate was filtered off
- customdried