Water → HCID 131725052, compound

HRID 583739Notes

Reaction equation

HRID 583739 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

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

  1. customTo a 2 liter glass vessel equipped with
  2. temperaturereflux condenser, stirrer
  3. additionwere charged
  4. temperaturethen heated to a gentle reflux
  5. customwas fed into the reactor over an approximate time frame of 3 hours
  6. 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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