反应详情

To 25.0 g (0.134 mol) of 2-(1-pyrrolidinyl)-2-(2-pyridyl)acetonitrile, prepared by the reaction of pyridine-2-carboxaldehyde with potassium cyanide and pyrrolidinium perchlorate, in 75 ml dry dimethylsulfoxide and 200 ml tetrahydrofuran at -10° was added 7.75 g (0.161 mol) of 50% sodium hydride dispersion. After no further gas evolution was observed, a solution of 22.34 g (0.161 mol) of methyl iodide in 10 ml tetrahydrofuran was added over a 10 minute period. After addition had been completed, the reaction mixture was warmed to 40° for two minutes and cooled to 15°. The reaction mixture was filtered and the precipitate was washed with methylene chloride. The filtrates were combined, washed with saturated sodium chloride solution, and dried over sodium sulfate. Removal of the solvent gave 24.75 g (92%) of the crude product, 2-(1-pyrrolidinyl)-2-(2-pyridyl)propionitrile. The total crude product was dissolved in 500 ml 95% ethanol, cooled to 5° and treated with 9.3 g (0.245 mol) sodium borohydride. The reaction mixture was stirred at room temperature for 20 hours and then filtered. Removal of the solvent at reduced pressure gave a tan oil which was dissolved in hexane and dried over sodium sulfate. The hexane solution was then filtered and concentrated. The crude product was distilled (78°-80°/0.2 mm Hg) to give 20.77 g (88%) of 1-(1-pyrrolidinyl)-1-(2-pyridyl)ethane.

1. additionAfter addition
2. temperaturethe reaction mixture was warmed to 40° for two minutes
3. temperaturecooled to 15°
4. filtrationThe reaction mixture was filtered
5. washthe precipitate was washed with methylene chloride
6. washwashed with saturated sodium chloride solution
7. dry with materialdried over sodium sulfate
8. customRemoval of the solvent
9. customgave 24.75 g (92%) of the crude product, 2-(1-pyrrolidinyl)-2-(2-pyridyl)propionitrile
10. temperaturecooled to 5°
11. filtrationfiltered
12. customRemoval of the solvent at reduced pressure
13. customgave a tan oil which
14. dry with materialdried over sodium sulfate
15. filtrationThe hexane solution was then filtered
16. concentrationconcentrated
17. distillationThe crude product was distilled (78°-80°/0.2 mm Hg)