反应详情

To a solution of 5-(3-methoxyphenyl)-2-pyrrolidinone (7.0 g) in dry tetrahydrofuran (280 ml) was added 1M lithium aluminum hydride in tetrahydrofuran (55 ml) dropwise at ambient temperature, under nitrogen. The reaction mixture was warmed under reflux for 21 hrs, cooled to ambient temperature, and quenched with 10% aqueous tetrahydrofuran (60 ml) followed by 10% sodium hydroxide solution (50 ml). The suspension was filtered through a pad of celite, and the filter cake was washed with dichloromethane. The combined filtrates were dried over anhydrous potassium carbonate, filtered, and concentrated to give 6.3 g (96%) of 2-(3-methoxyphenyl)pyrrolidine.

1. temperatureThe reaction mixture was warmed
2. temperatureunder reflux for 21 hrs
3. customquenched with 10% aqueous tetrahydrofuran (60 ml)
4. filtrationThe suspension was filtered through a pad of celite
5. washthe filter cake was washed with dichloromethane
6. dry with materialThe combined filtrates were dried over anhydrous potassium carbonate
7. filtrationfiltered
8. concentrationconcentrated