Benzoyl Peroxide → HCID 21225556, compound

HRID 1941053Notes

Reaction equation

HRID 1941053 reaction equation
[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O:13]CCCC)(=[O:12])[CH:10]=[CH2:11].C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1>C1(C)C(C)=CC=CC=1>[CH2:1]=[CH:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[C:9]([O-:13])(=[O:12])[CH:10]=[CH2:11]

Participants

5

Reactant 3

HCID 7187Benzoyl PeroxideHCID 7501StyreneHCID 8846Butyl Acrylate

Product 1

HCID 21225556HCID 21225556, compound

Reagents, catalysts & solvents 1

HCID 7237O-XyleneSolvent4×

Procedure

15 Parts of the above-obtained polymer resin having a higher molecular weight and 100 parts of xylene were charged into a flask, and dissolved. The inner atmosphere of the flask was replaced with nitrogen gas, and the mixture was heated up to the boiling point of xylene. While the mixture was stirred under the reflux of xylene, a mixture containing 72 parts of styrene, 13 parts of n-butyl acrylate and 3.3 parts of benzoyl peroxide (polymerization initiator) were dropwise added over 2 hours to carry out a solution polymerization. After the addition was completed, the reaction mixture was aged for 1 hour with stirring under the reflux of xylene, to give a styrene/acrylate copolymer resin having molecular weight maximal values, measured by GPC, of 6,000 and 1.2×106 and containing 15% by weight of the polymer having a higher molecular weight, for use in an electrophotographic toner of the present invention.

Workup

  1. additionwere charged into a flask
  2. dissolutiondissolved
  3. additionwere dropwise added over 2 hours
  4. customa solution polymerization
  5. additionAfter the addition
  6. stirringwith stirring under the

Sources & evidence

ORD record
ord-21a69eb60d2d4148bd5186bb22f0be3c
Source dataset
uspto-grants-1997_12
Patent number
US05702859

Reaction notes

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