Reaktion #1375845

ord-739b44e7be3e4c898fc416a51be11bad

Reaktionsgleichung

[Na+].c1cc[cH-]c1
sodium cyclopentadienylide
CCC=CC1=CCC=C1
colourless oil
Ausbeute 69.0%
CCC=CC1=CCC=C1
3-butenylcyclopentadiene
Ausbeute 69.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto warm to room temperature
  2. 2
    Extraktionthe product extracted with ether (3×75 ml)
  3. 3
    TrocknenThe combined organic fractions were dried over magnesium sulphate for 2 hours
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigethe solvents removed under reduced pressure
  6. 6
    Sonstigea rotary evaporator
  7. 7
    Sonstigeto yield a dark brown oil
  8. 8
    workup.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%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05747405uspto-grants-1998_05