تفاعل #1508312

ord-aff45d2b0c5b462f895a0ee71b2abf35

الكواشف

المذيبات

ظروف التفاعل

درجة الحرارة
10°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA double-walled reactor having
  2. 2
    أخرىa volume of 1.5 L, provided with baffles, condenser, top stirrer
  3. 3
    workup.STIRRINGAfter one hour of stirring at room temperature
  4. 4
    درجة الحرارةthe reaction mixture was heated to 35° C.
  5. 5
    workup.STIRRINGof stirring
  6. 6
    workup.STIRRINGStirring
  7. 7
    أخرىphase separation
  8. 8
    workup.ADDITION920 g (11.5 mol) of fresh 50% strength NaOH were added
  9. 9
    workup.WAITfollowed by a further 5 hours
  10. 10
    workup.STIRRINGof stirring at room temperature
  11. 11
    workup.DISTILLATIONThe product was distilled under reduced pressure
  12. 12
    workup.DISTILLATIONAfter vacuum distillation

الإجراء التجريبي

A double-walled reactor having a volume of 1.5 L, provided with baffles, condenser, top stirrer, thermometer and dropping funnel, was charged with 900 g of clear 50% strength NaOH (11.3 mol), followed by cooling to 10° C. Then 30 g of Aliquat 336 (74 mmol) and 48 g (0.72 mol) of freshly cracked cyclopentadiene were added. The reaction mixture was stirred vigorously for a few minutes, then 577 g of octyl bromide (2.99 mol) were added over a period of one hour, while the reaction mixture was cooled with circulating water at 10° C. After one hour of stirring at room temperature, the reaction mixture was heated to 35° C., followed by a further 6 hours of stirring. Stirring was stopped and phase separation was performed. The aqueous layer was drawn off and 920 g (11.5 mol) of fresh 50% strength NaOH were added, followed by a further 5 hours of stirring at room temperature. GC was used to show that 10% of tri-, 83% of tetra- and 7% of penta(octyl)cyclopentadiene were present in the mixture. The product was distilled under reduced pressure. After vacuum distillation, 226.6 g of tetra(octyl)cyclopentadiene were obtained, which was characterized with GC, GC-MS, 13C- and 1H-NMR.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06072067uspto-grants-2000_06