Reaktion #1106657

ord-ea3f6c2c23104378aaa9f357bc1df208

Reaktionsgleichung

[Na+].[OH-]
NaOH
CCCCO
BuOH
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

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONcharged to an appropriately sized reaction vessel
  2. 2
    SonstigeThe solution was sparged with nitrogen for 10 min
  3. 3
    Sonstigeto remove oxygen
  4. 4
    workup.ADDITIONafter which the solution was diluted to 20 wt % with 181.3 g of THF
  5. 5
    workup.ADDITIONwere mixed at 70° C. for 1 hr
  6. 6
    workup.STIRRINGto stir for 2 hr at 70° C.
  7. 7
    Temperaturwas cooled to room temperature
  8. 8
    workup.ADDITIONThe reaction mixture was treated with cone
  9. 9
    WaschenHClaq for protonation, and then washed three times
  10. 10
    Sonstigeto remove residual salts and acid
  11. 11
    SonstigeThe organic phase was separated
  12. 12
    Einengenconcentrated in vacuo
  13. 13
    workup.DISSOLUTIONredissolved in THF
  14. 14
    Sonstigeto form an approximately 20 wt % copolymer solution
  15. 15
    Sonstigethe copolymer was precipitated
  16. 16
    workup.ADDITIONby adding the THF solution to hexane (20 fold excess)
  17. 17
    SonstigeThe copolymer was separated by filtration
  18. 18
    Sonstigedried in a vacuum oven at 80° C. for 16 hr

Vorschrift

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 THF (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 23 hr, after which the solution was diluted to 20 wt % with 181.3 g of THF. The resulting solution was added to the suspension of NaOH (8.8 g, 220 mmol), BuOH (74.0 g, 1 mol) and THF (80.0 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. 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, 44.4 g (75%) of the ROMA copolymer of MA/PENB with BuOH was isolated (GPC Mw=7,700 Mn=4,000).

Quelle

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