Azobisisobutyronitrile → 2-Hydroxyethyl Methacrylate
Reaction equation
[CH3:1][C:2]([C:4]([O:6][CH2:7][CH2:8][O:9]C)=[O:5])=[CH2:3].CC(N=NC(C#N)(C)C)(C#N)C>C1(C)C(C)=CC=CC=1>[CH3:3][C:2]([C:4]([O:6][CH2:7][CH2:8][OH:9])=[O:5])=[CH2:1]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
A 0.5% of aqueous solution of 88% hydrolyzed polyvinylalcohol (90 ml) was introduced into a 100 ml reactor and allowed to stand under a nitrogen atmosphere for 15 min. The monomer phase containing poly(ethylene glycol)methyl ether methacrylate (2.77 g), PLA cross-linker (0.7 g) and 1 wt % AIBN solubilized in 4.3 ml of xylene was degassed by bubbling nitrogen through the solution for 15 min. The monomer phase was added to the aqueous phase at 50° C. and agitated by means of a propeller type stirrer at an appropriate velocity so as to obtain monomer droplets of desired diameter. The temperature was increased to 80° C. and stirred for 5 h. The mixture was filtered hot and washed with water and acetone. Then, beads were freeze dry. Size 390±100 μm.
Workup
- customwas degassed
- customby bubbling nitrogen through the solution for 15 min
- additionThe monomer phase was added to the aqueous phase at 50° C.
- customto obtain monomer droplets of desired diameter
- stirringstirred for 5 h
- filtrationThe mixture was filtered hot
- washwashed with water and acetone
- customdry
Sources & evidence
- ORD record
- ord-9dfdaea740cf42338ba5a05abfeb52e9
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09320804B2
Reaction notes
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