Sodium Hydroxide → HCID 86735496, compound

HRID 616803Notes

Reaction equation

HRID 616803 reaction equation
[CH:1]([N:3]1[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:9]2[C:4]1=[CH:5][CH:6]=[CH:7][CH:8]=2)=[CH2:2].[C:16](OC=C)(=[O:18])[CH3:17].[OH-].[Na+].C(N1C2C=CC=CC=2C2C1=CC=CC=2)=C>O1CCCC1>[CH:1]([N:3]1[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:9]2[C:4]1=[CH:5][CH:6]=[CH:7][CH:8]=2)=[CH2:2].[CH:16]([OH:18])=[CH2:17]

Participants

5

Reactant 3

HCID 14798Sodium HydroxideHCID 15143N-VinylcarbazoleHCID 86735497HCID 86735497, compound

Product 1

HCID 86735496HCID 86735496, compoundYield 90%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
60 °C

Procedure

Copoly(N-vinyl carbazole-vinyl acetate) (5.0 g) was dissolved in 100 ml of tetrahydrofuran and 25 ml of I N methanolic sodium hydroxide was added. The solution was stirred for 3 hours at 60° C and precipitated into 600 ml of methanol. The polymer was purified by two additional precipitations from tetrahydrofuran into methanol. The purified polymer was obtained in 90% yield and was found to contain 46.6 mole percent N-vinyl carbazole (calculated from nitrogen analysis).

Workup

  1. customprecipitated into 600 ml of methanol
  2. customThe polymer was purified by two additional precipitations from tetrahydrofuran into methanol
  3. customThe purified polymer was obtained in 90% yield

Sources & evidence

ORD record
ord-e6ce1db0520742279276520a5630c26e
Source dataset
uspto-grants-1978_02
Patent number
US04076526

Reaction notes

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