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
A flask was charged with 4-bromo-2-nitroaniline (505 mg), potassium (2-(((benzyloxy)carbonyl)amino)ethyl)trifluoroborate (745 mg), Pd(OAc)2 (25.3 mg), 2-(dicyclohexylphosphino)-2′,6′-dimethoxybiphenyl (94.6 mg) and Cs2CO3 (2.2 g) in dioxane/water (20 mL/2 mL). The reaction mixture was refluxed for 92 h, cooled down, diluted with EA and washed with water and brine. The aq. layers were extracted with EA, the combined org. layers were dried (MgSO4), filtered off and evaporated to dryness. The residue was purified by CC (Biotage, SNAP 25 g cartridge, solvent A: Hept; solvent B: EA; gradient in % B: 10 for 3CV, 10 to 30 over 3CV, 30 for 4CV, 30 to 50 over 3CV, 50 for 5CV) to afford 143 mg of red oil. LC-MS (B): tR=0.85 min; [M]+: 316.07.
WORKUP
后处理
- temperatureThe reaction mixture was refluxed for 92 h
- temperaturecooled down
- washwashed with water and brine
- extractionThe aq. layers were extracted with EA
- dry with materiallayers were dried (MgSO4)
- filtrationfiltered off
- customevaporated to dryness
- customThe residue was purified by CC (Biotage, SNAP 25 g cartridge, solvent A: Hept; solvent B: EA; gradient in % B: 10 for 3CV, 10 to 30 over 3CV, 30 for 4CV, 30 to 50 over 3CV, 50 for 5CV)