Water → HCID 131725052, compound
Reaction equation
O.[C:2]([O:7][CH2:8][CH2:9][N:10]([CH3:12])[CH3:11])(=[O:6])[C:3]([CH3:5])=[CH2:4].[C:13]([O:17][CH2:18][CH3:19])(=[O:16])[CH:14]=C.S(OOS([O-])(=O)=O)([O-])(=O)=O.[Na+].[Na+]>CC(O)C>[CH3:5][C:3]([C:2]([O:7][CH2:8][CH2:9][N:10]([CH3:12])[CH3:11])=[O:6])=[CH2:4].[CH3:14][C:13](=[O:16])[O:17][CH2:18][CH3:19]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a 2 liter glass vessel equipped with; reflux condenser, stirrer, means of temperature control, 300 g deionized water and 300 g propan-2-ol were charged then heated to a gentle reflux. A monomer mixture of dimethylaminoethyl methacrylate (134.6 g) and ethyl acrylate (200 g) was fed into the reactor over an approximate time frame of 3 hours. Sodium persulphate solution (3.4 g in 125 g of water) was fed concurrently with the monomer over a similar time period. When feeds were a propan-2-ol azeotrope was then distilled from the reactor, followed by neutralization with acetic acid (41.2 g).
Workup
- customTo a 2 liter glass vessel equipped with
- temperaturereflux condenser, stirrer
- additionwere charged
- temperaturethen heated to a gentle reflux
- customwas fed into the reactor over an approximate time frame of 3 hours
- distillationwas then distilled from the reactor
Sources & evidence
- ORD record
- ord-ae67b3922d5f42a298b82c26ba1d8de8
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06924259B2
Reaction notes
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