Methacrylic Acid → 1-Benzyloxyethyl methacrylate 2-hydroxyethyl methacrylate methacrylic acid

HRID 574019ノート

反応式

HRID 574019 の反応式
[C:1]([O:6][CH:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:8])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:17]([O:22][CH2:23][CH2:24][OH:25])(=[O:21])[C:18]([CH3:20])=[CH2:19].[C:26]([OH:31])(=[O:30])[C:27]([CH3:29])=[CH2:28].N(C(C)(CC)C([O-])=O)=NC(C)(CC)C([O-])=O>CCCCCCC.C(C(C)=O)C(C)C>[C:1]([O:6][CH:7]([O:9][CH2:10][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)[CH3:8])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:17]([O:22][CH2:23][CH2:24][OH:25])(=[O:21])[C:18]([CH3:20])=[CH2:19].[C:26]([OH:31])(=[O:30])[C:27]([CH3:29])=[CH2:28]

参加物

7

実験手順

Into a 500 ml-volume three-neck flask, 105.7 g (0.48 mol) of 1-benzyloxyethyl methacrylate, 7.8 g (0.06 mol) of 2-hydroxyethyl methacrylate, 5.2 g (0.06 mol) of methacrylic acid and 300 ml of methyl isobutyl ketone were charged. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) was added thereto as a radical polymerization initiator, and polymerization was allowed to proceed at 80° C. for 6 hours in a nitrogen stream. The reaction solution was cooled and then poured in a large amount of heptane to precipitate a polymer. The crystal was collected by filtration and dissolved in diethylene glycol dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A1-2 (1-benzyloxyethyl methacrylate/2-hydroxyethyl methacrylate/methacrylic acid) as a diethylene glycol dimethyl ether solution.

後処理

  1. customas a radical polymerization initiator, and polymerization
  2. temperatureThe reaction solution was cooled
  3. customto precipitate a polymer
  4. filtrationThe crystal was collected by filtration
  5. dissolutiondissolved in diethylene glycol dimethyl ether
  6. customwere removed by distillation under reduced pressure

出典と根拠

ORDレコード
ord-cf309c1a6bf941d79e0d7978673811a5
出典データセット
uspto-grants-2015_05
特許番号
US09034440B2

反応ノート

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