Acrylic Acid → Phenoxyethyl acrylate methyl methacrylate acrylic acid

HRID 1639471Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1639471
[C:1]([O:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:4])[CH:2]=[CH2:3].[C:15]([O:20][CH3:21])(=[O:19])[C:16]([CH3:18])=[CH2:17].[C:22]([OH:26])(=[O:25])[CH:23]=[CH2:24].N(C(C)(C)C(OC)=O)=NC(C)(C)C(OC)=O>C(O)(C)C.C(C(C)=O)C>[C:1]([O:5][CH2:6][CH2:7][O:8][C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)(=[O:4])[CH:2]=[CH2:3].[C:15]([O:20][CH3:21])(=[O:19])[C:16]([CH3:18])=[CH2:17].[C:22]([OH:26])(=[O:25])[CH:23]=[CH2:24]

Komponenten

7

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

360.0 g of methyl ethyl ketone was charged in a 2 litter three-necked flask equipped with a stirrer, a thermometer, a reflux cooling tube, and a nitrogen gas introduction tube, and the temperature was elevated to 75° C. Then, while keeping the temperature inside the flask at 75° C., a solution mixture of 180.0 g of phenoxyethyl acrylate, 162.0 g of methyl methacrylate, 18.0 g of acrylic acid, 72 g of methyl ethyl ketone, and 1.44 g of “V-601” (manufactured by Wako Pure Chemical Industries, Ltd.) was dropped at a constant speed so as to complete dropping in 2 hr. After completion of the dropping, a solution of 0.72 g of “V-601” and 36.0 g of methyl ethyl ketone was added, stirred at 75° C. for 2 hr and then, a solution of 0.72 g of “V-601” and 36.0 g of isopropanol was further added and stirred at 75° C. for 2 hr. Then, the temperature was elevated to 85° C. and stirring was continued for further 2 hr, thereby obtaining a resin solution of phenoxyethyl acrylate/methyl methacrylate/acrylic acid (=50/45/5 [mass ratio]) copolymer.

Aufarbeitung

  1. customequipped with a stirrer
  2. temperaturea thermometer, a reflux cooling tube, and a nitrogen gas introduction tube
  3. customwas elevated to 75° C
  4. customat 75° C.
  5. additionwas dropped at a constant speed so as
  6. stirringstirred at 75° C. for 2 hr
  7. customwas elevated to 85° C.
  8. stirringstirring
  9. waitwas continued for further 2 hr

Quellen und Nachweise

ORD-Eintrag
ord-8cd0e862ac6748d4a85c4c832bee7e5b
Quelldatensatz
uspto-grants-2012_02
Patentnummer
US08109623B2

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