Reaction #1106658

ord-3f83889be3314269a86fcb65a87f3a66

Reaction equation

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
[Na+].[OH-]
NaOH
CCCCO
BuOH
CCC12CCC(C=C1c1ccccc1)C2.O=C1C=CC(=O)O1
MA PENB

Solvents

Conditions

Temperature
60°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONcharged to an appropriately sized reaction vessel
  2. 2
    OtherThe solution was sparged with nitrogen for 10 min
  3. 3
    Otherto remove oxygen
  4. 4
    ConcentrationThe 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 2 hr at 70° C.
  8. 8
    Temperaturewas cooled to room temperature
  9. 9
    workup.ADDITIONThe reaction mixture was treated with cone
  10. 10
    WashHClacq for protonation, and then washed three times
  11. 11
    Otherto remove residual salts and acid
  12. 12
    OtherThe organic phase was separated
  13. 13
    Concentrationconcentrated in vacuo
  14. 14
    workup.DISSOLUTIONredissolved in THF
  15. 15
    Otherto form an approximately 20 wt % copolymer solution
  16. 16
    Otherthe copolymer was precipitated
  17. 17
    workup.ADDITIONby adding the THF solution to hexane (20 fold excess)
  18. 18
    OtherThe copolymer was separated by filtration
  19. 19
    Otherdried in a vacuum oven at 80° C. for 16 hr

Procedure

Maleic Anhydride (MA, 19.6 g, 200.0 mmol), Phenyl Ethyl Norbornene (PENB, 39.6 g, 200 mmol) and AIBN (3.3 g, 20.0 mmol) was dissolved in EtOAc (36.2 g) and charged to an appropriately sized 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 20 hr. The reaction mixture was concentrated in vacuo and redissolved in THF (20 wt %). The resulting solution was added to the suspension of NaOH (8.80 g, 220 mmol), BuOH (74.12 g, 1 mol) and TI-IF (74.12 g) which were mixed at 70° C. for 1 hr. The mixture was allowed to stir for 2 hr at 70° C. and then was cooled to room temperature. The reaction mixture was treated with cone. HClacq 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, 37.5 g (51%) of the ROMA copolymer of MA/PENB with BuOH was isolated (GPC Mw=9,900 Mn=5,400).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08715900B2uspto-grants-2014_05