Реакция #1106660

ord-a5d919d51abb42b7a91c2adee1bd516e

Уравнение реакции

[Na+].[OH-]
NaOH
CO
MeOH
O=C1C=CC(=O)O1
Maleic Anhydride
CCC12CCC(C=C1c1ccccc1)C2
Phenyl Ethyl Norbornene
CC(C)(C#N)N=NC(C)(C)C#N
AIBN
CCC12CCC(C=C1c1ccccc1)C2.O=C1C=CC(=O)O1
MA PENB

Реагенты

Нет

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONcharged to a reaction vessel
  2. 2
    ДругоеThe solution was sparged with nitrogen for 10 min
  3. 3
    Другоеto remove oxygen
  4. 4
    КонцентрированиеThe reaction mixture was concentrated in vacuo
  5. 5
    workup.DISSOLUTIONredissolved in THF (20 wt %)
  6. 6
    workup.ADDITIONwere mixed at 70° C. for 1 hr
  7. 7
    workup.STIRRINGto stir for 3 hr at 70° C.
  8. 8
    Температураwas cooled to room temperature
  9. 9
    workup.ADDITIONThe reaction mixture was treated with conc. HClaq for protonation
  10. 10
    Промывкаwashed three times
  11. 11
    Другоеto remove residual salts and acid
  12. 12
    ДругоеThe organic phase was separated
  13. 13
    Концентрированиеconcentrated in vacuo
  14. 14
    workup.DISSOLUTIONredissolved in THF
  15. 15
    Другоеto form an approximately 20 wt % copolymer solution
  16. 16
    Другоеthe copolymer was precipitated
  17. 17
    workup.ADDITIONby adding the THF solution to hexane (20 fold excess)
  18. 18
    ДругоеThe copolymer was separated by filtration
  19. 19
    Другоеdried in a vacuum oven at 80° C. for 16 hr

Методика

Maleic Anhydride (MA, 14.7 g, 150 mmol), Phenyl Ethyl Norbornene (PENB, 29.7 g, 150 mmol) and AIBN (2.5 g, 15.0 mmol) was dissolved in EtOAc (27.1 g) and charged to a reaction vessel. The solution was sparged with nitrogen for 10 min to remove oxygen and then heated to 60° C. The mixture was allowed to stir at 60° C. for 24 hr. The reaction mixture was concentrated in vacuo and redissolved in THF (20 wt %). The resulting solution was added to the suspension of NaOH (6.6 g, 165 mmol), MeOH (24.0 g, 750 mmol) and THF (24.0 g) which were mixed at 70° C. for 1 hr. The mixture was allowed to stir for 3 hr at 70° C. and then was cooled to room temperature. The reaction mixture was treated with conc. HClaq for protonation, and then washed three times to remove residual salts and acid. The organic phase was separated and then concentrated in vacuo, redissolved in THF to form an approximately 20 wt % copolymer solution and then the copolymer was precipitated by adding the THF solution to hexane (20 fold excess). The copolymer was separated by filtration and dried in a vacuum oven at 80° C. for 16 hr. Approximately, 30.4 g (61%) of the Ring-opening polymer of MA/PENB with MeOH was isolated (GPC Mw=9,700 Mn=5,300).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08715900B2uspto-grants-2014_05