15023-39-9 → HCID 86756712, compound

HRID 1978101Notes

Reaction equation

HRID 1978101 reaction equation
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2[CH2:8][NH:9][S:10]([CH2:13][CH2:14][CH3:15])(=[O:12])=[O:11].[C:16]12([C:23]([OH:25])=[O:24])[CH2:22][CH:19]([CH2:20][CH2:21]1)[CH:18]=[CH:17]2>C1(C)C=CC=CC=1.O1CCCC1>[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH:2]2[CH2:8][NH:9][S:10]([CH2:13][CH2:14][CH3:15])(=[O:12])=[O:11].[C:16]12([C:23]([OH:25])=[O:24])[CH2:22][CH:19]([CH2:20][CH2:21]1)[CH:18]=[CH:17]2

Participants

5

Reactant 2

HCID 1785159515023-39-9HCID 18468854N-(Bicyclo[2.2.1]hept-5-en-2-ylmethyl)-1-propanesulfonamide

Product 1

HCID 86756712HCID 86756712, compound

Reagents, catalysts & solvents 2

HCID 1140TolueneSolvent2×HCID 8028TetrahydrofuranSolvent

Procedure

To a glass vial containing a stir bar was added under nitrogen atmosphere 13.04 g (0.069 mol.) of N-(bicyclo(2.2.1)hept-5-ene-2-ylmethyl) propanesulfonamide, 21.96 g (0.104 mol.) of trimethylsilyl ester of norbornene carboxylic acid, followed by 85 ml of toluene. The reaction mixture was purged with Argon for 10 minutes. To the reaction solution at room temperature was added via syringe the nickel catalyst solution in a monomer to catalyst ratio of 50/1. The catalyst solution was prepared inside the dry box by adding 1.7 g (3.49 mmol.) (CH3C6H4)Ni(PhF5)2 in 5 ml of toluene. The polymerization was allowed to stir for 6 hours after which the solution was diluted with tetrahydrofuran. The resulting polymer solution was treated first with preconditioned imidoacetic acid based Amberlite IRC-718 chelating resin, followed by Sulfonic acid based Amberlyst 18 ion exchange resin. The polymer solution is filtered, concentrated via rotary evaporation and precipitated into methyl t-butyl ether. The precipitated polymer was filtered, redissolved tetrahydrofuran and reprecipitated into methyl t-butyl ether. The precipitated polymer is filtered and dried overnight under reduced pressure. The overall yield of polymer was 12 g (35%). The polymer was further characterized using GPC, IR and NMR. IR and 1H NMR clearly indicated presence of sulfonamide and carboxylic acid group.

Workup

  1. additionTo a glass vial containing a stir bar
  2. customThe reaction mixture was purged with Argon for 10 minutes
  3. additionTo the reaction solution at room temperature was added via syringe the nickel catalyst solution in a monomer to catalyst ratio of 50/1
  4. customThe catalyst solution was prepared inside the dry box
  5. filtrationThe polymer solution is filtered
  6. concentrationconcentrated via rotary evaporation
  7. customprecipitated into methyl t-butyl ether
  8. filtrationThe precipitated polymer was filtered
  9. dissolutionredissolved tetrahydrofuran
  10. customreprecipitated into methyl t-butyl ether
  11. filtrationThe precipitated polymer is filtered
  12. customdried overnight under reduced pressure

Sources & evidence

ORD record
ord-ed052a5ec0a04e9481709e7a84c7b000
Source dataset
uspto-grants-2001_05
Patent number
US06235849B1

Reaction notes

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