Methacrylic Acid → Benzoyl Peroxide

HRID 1885049Notes

Reaction equation

HRID 1885049 reaction equation
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH2:7]=[CH:8][C:9]1C=CC=CC=1.[C:15]([O:20]CC(C)C)(=[O:19])[C:16]([CH3:18])=[CH2:17].[C:25](OCCO)(=O)[C:26](C)=[CH2:27].C1(=O)OCCCCC1>C(OCC)(=O)C>[C:1]([O:6][O:20][C:15](=[O:19])[C:16]1[CH:17]=[CH:27][CH:26]=[CH:25][CH:18]=1)(=[O:5])[C:2]1[CH:4]=[CH:9][CH:8]=[CH:7][CH:3]=1

Participants

7

Procedure

Subsequently, 100 parts of the resin (VIB-3) was fed into a same reaction vessel replaced with nitrogen, followed by elevating a temperature to 75° C. while agitating. There was added dropwise a mixture composed of 15.4 parts of methacrylic acid, 23.3 parts of styrene, 22.4 parts of isobutyl methacrylate, 5.5 parts of 2-hydroxyethyl methacrylate, 50.1 parts of the -caprolactone-modified acrylic monomer obtained in the Reference Example 3, 9.3 parts of “Niper BW” [benzoyl peroxide manufactured by Nihon Yushi, Ltd.], and 116.7 parts of ethyl acetate over 4 hours to allow to conduct a polymerization reaction. Also after that, agitation was allowed to continue over 4 hours to obtain a vinyl-based copolymer (VIA-5). Nonvolatile components were 48.6%.

Workup

  1. customSubsequently, 100 parts of the resin (VIB-3) was fed into a same reaction vessel
  2. customto 75° C.
  3. additionThere was added dropwise a mixture

Sources & evidence

ORD record
ord-b72cea508b91433ca154f45d7033aa1d
Source dataset
uspto-grants-2004_07
Patent number
US06767987B2

Reaction notes

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