Реакция #1755453

Уравнение реакции

glycidyl methacrylate

Vazo 64

tetrahydrofuran

N,N-dimethylacrylamide

→

DMA GMA

Растворители

ether

Условия реакции

Обработка

1. 1
   ДругоеTo a 1 L reaction flask
2. 2
   workup.ADDITIONwere added
3. 3
   ДругоеThe reaction vessel was fitted with a mechanical stirrer, condenser
4. 4
   ДругоеNitrogen was bubbled through the solution for 15 minutes
5. 5
   Другоеto remove any dissolved oxygen
6. 6
   workup.ADDITIONThe reaction mixture was then added slowly to ethyl ether (1.5 L) with good mechanical stirring
7. 7
   ДругоеThe reactive polymer precipitated
8. 8
   Другоеorganic solvents were decanted off
9. 9
   ФильтрацияThe solid was collected by filtration

Методика

The DMA/GMA copolymer of Example 13 was prepared by the following procedure. To a 1 L reaction flask were added distilled N,N-dimethylacrylamide (DMA, 48 g, 0.48 moles), distilled glycidyl methacrylate (GMA, 12 g, 0.08 moles) Vazo 64 initiator (AIBN, 0.1 g, 0.0006 moles) and anhydrous tetrahydrofuran (500 ml). The reaction vessel was fitted with a mechanical stirrer, condenser, thermal controller and a nitrogen inlet. Nitrogen was bubbled through the solution for 15 minutes to remove any dissolved oxygen. The reaction flask was then heated to 40° C. under a passive blanket of nitrogen for 168 hours. The reaction mixture was then added slowly to ethyl ether (1.5 L) with good mechanical stirring. The reactive polymer precipitated and organic solvents were decanted off. The solid was collected by filtration and placed in a vacuum oven to remove the ether leaving 58.2 g of reactive polymer (97% yield). The reactive polymer was placed in a desiccator for storage until use.

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