Reacción #1106657

ord-ea3f6c2c23104378aaa9f357bc1df208

Ecuación de reacción

[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

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08715900B2uspto-grants-2014_05