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
CONDITIONS
反应条件
- 温度
- 50 °C
PROCEDURE
实验过程
A 200-mL round-bottomed flask equipped with mechanical stirrer was charged with 5-Methyl-4-nitro-1-(pyridin-4-yl)methyl-1H-benzimidazole (881 mg, 3.46 mmol), iron powder (˜325 mesh, 3.87 g, 6.92 mmol) and acetic acid (50 mL), and the resulting mixture stirred at 50° C. for 15 min. After this time the reaction was cooled to room temperature, diluted with 1:1 methylene chloride/methanol (1 L) and filtered through a pad of Celite 521. After washing the filter cake with 1:1 methylene chloride/methanol (2×50 mL), the filtrate was concentrated in vacuo. The resulting residue was dissolved in methylene chloride (50 mL) and vigorously stirred with 1M aqueous sodium hydroxide (50 mL). The resulting emulsion was filtered through a pad of Celite 521, the pad washed with methylene chloride (2×25 mL) and the organic layer of the filtrate separated and dried over sodium sulfate. Removal of the drying agent by filtration, followed by evaporation of the filtrate in vacuo gave a residue which was purified by flash chromatography. This purified material was dissolved in warm methylene chloride (15 mL) and the solution diluted with hexanes (35 mL). The resulting precipitate was filtered, washed with hexanes (3×100 mL) and dried under reduced pressure for 1.5 h to afford compound 2d as an off-white solid.
WORKUP
后处理
- customA 200-mL round-bottomed flask equipped with mechanical stirrer
- temperatureAfter this time the reaction was cooled to room temperature
- filtrationfiltered through a pad of Celite 521
- washAfter washing the filter cake with 1:1 methylene chloride/methanol (2×50 mL)
- concentrationthe filtrate was concentrated in vacuo
- dissolutionThe resulting residue was dissolved in methylene chloride (50 mL)
- stirringvigorously stirred with 1M aqueous sodium hydroxide (50 mL)
- filtrationThe resulting emulsion was filtered through a pad of Celite 521
- washthe pad washed with methylene chloride (2×25 mL)
- customthe organic layer of the filtrate separated
- dry with materialdried over sodium sulfate
- customRemoval of the drying agent
- filtrationby filtration
- customfollowed by evaporation of the filtrate in vacuo
- customgave a residue which
- customwas purified by flash chromatography
- dissolutionThis purified material was dissolved in warm methylene chloride (15 mL)
- additionthe solution diluted with hexanes (35 mL)
- filtrationThe resulting precipitate was filtered
- washwashed with hexanes (3×100 mL)
- customdried under reduced pressure for 1.5 h