تفاعل #1106657

ord-ea3f6c2c23104378aaa9f357bc1df208

معادلة التفاعل

[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

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08715900B2uspto-grants-2014_05