Reaktion #1375845
ord-739b44e7be3e4c898fc416a51be11bad
Reaktionsgleichung
sodium cyclopentadienylide
→
colourless oil
Ausbeute 69.0%
3-butenylcyclopentadiene
Ausbeute 69.0%
Reagenzien
Keine
Reaktionsbedingungen
Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturto warm to room temperature
- 2Extraktionthe product extracted with ether (3×75 ml)
- 3TrocknenThe combined organic fractions were dried over magnesium sulphate for 2 hours
- 4Filtrationfiltered
- 5Sonstigethe solvents removed under reduced pressure
- 6Sonstigea rotary evaporator
- 7Sonstigeto yield a dark brown oil
- 8workup.DISTILLATIONThe crude product was distilled under reduced pressure (b.p. 50°-51° C. @ 15 mm Hg)
Vorschrift
To a solution of 25.0 g (110 mmol) 3-buten-1-tosylate prepared according to step (a) above in 200 ml THF cooled to 0° C. was added 68.9 ml of 2.0 M (138 mmol) sodium cyclopentadienylide in THF. The reaction mixture was allowed to warm to room temperature and was stirred for 16 h. 100 ml concentrated aqueous saline solution was added and the product extracted with ether (3×75 ml). The combined organic fractions were dried over magnesium sulphate for 2 hours, filtered and the solvents removed under reduced pressure using a rotary evaporator to yield a dark brown oil. The crude product was distilled under reduced pressure (b.p. 50°-51° C. @ 15 mm Hg) to give 5.71 g of a colourless oil (47.6 mmol, 43.3%).