反应详情

c is-1-Benzyl-4-methyl-3-aminomethylpyrrolidine (1000 mg) was dissolved in methanol (10 mL). While this solution was cooled on an ice bath, benzaldehyde (0.50 mL) was added dropwise and the mixture was stirred at room temperature for 1 hour. Subsequently, sodium cyanoborohydride (184 mg) was added and the mixture was stirred at room temperature for 1.5 hours. This was followed by a second addition of sodium cyanoborohydride (123 mg) and stirring for additional 5.5 hours. Subsequently, a 2mol/L aqueous solution of sodium hydroxide (5 mL) was added to the reaction mixture and the mixture was refluxed for 2 hours while heated. Following concentration under reduced pressure, the resulting residue was extracted with toluene (2×30 mL) and the toluene extracts were combined. The combined toluene layer was then washed with water, followed by drying over anhydrous sodium sulfate and concentration under reduced pressure. The resulting residue was purified on a silica gel column (hexane:ethyl acetate=4:1) to give 690 mg of cis-1-benzyl-3-benzylaminomethyl-4-methylpyrrolidine as a pale yellow oil.

1. temperatureWhile this solution was cooled on an ice bath
2. stirringthe mixture was stirred at room temperature for 1.5 hours
3. stirringstirring for additional 5.5 hours
4. temperaturethe mixture was refluxed for 2 hours
5. temperaturewhile heated
6. concentrationconcentration under reduced pressure
7. extractionthe resulting residue was extracted with toluene (2×30 mL)
8. washThe combined toluene layer was then washed with water
9. dry with materialby drying over anhydrous sodium sulfate and concentration under reduced pressure
10. customThe resulting residue was purified on a silica gel column (hexane:ethyl acetate=4:1)