Water → Tetrahydropyranyl acrylate methyl methacrylate

HRID 2675

反応式

HRID 2675 の反応式
[C:1]([O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][O:7]1)(=[O:4])[CH:2]=[CH2:3].[C:12]([O:17][CH3:18])(=[O:16])[C:13]([CH3:15])=[CH2:14].N(C(C)(C)C#N)=NC(C)(C)C#N.O>COCC(O)C>[C:1]([O:5][CH:6]1[CH2:11][CH2:10][CH2:9][CH2:8][O:7]1)(=[O:4])[CH:2]=[CH2:3].[C:12]([O:17][CH3:18])(=[O:16])[C:13]([CH3:15])=[CH2:14]

参加物

6

反応物 4

HCID 962WaterHCID 6547AzobisisobutyronitrileHCID 6658Methyl MethacrylateHCID 21909470Oxan-2-yl prop-2-enoate

生成物 1

HCID 86752303Tetrahydropyranyl acrylate methyl methacrylate

試薬・触媒・溶媒 1

HCID 79001-Methoxy-2-propanol溶媒

実験手順

In 80 g of propylene glycol monomethyl ether were dissolved 78 g (0.5 mole) of tetrahydropyranyl acrylate and 42 g (0.5 mole) of methyl methacrylate, and 3 g of azobisisobutyronitrile was added thereto, after which they were subjected to polymerization for 10 hours under a nitrogen atmosphere while the reaction temperature was kept at 80° C. After the polymerization, the reaction mixture was dropped into a large amount of water to coagulate a resin. The resin was recovered and dried in a vacuum drier kept at 50° C. overnight to obtain 96 g of a white fine powder of tetrahydropyranyl acrylate/methyl methacrylate copolymer resin.

後処理

  1. additionwas added
  2. customafter which they were subjected to polymerization for 10 hours under a nitrogen atmosphere while the reaction temperature
  3. customwas kept at 80° C
  4. customAfter the polymerization
  5. customThe resin was recovered
  6. customdried in a vacuum drier

出典と根拠

ORDレコード
ord-71f52937412841d2816b018d6d494dfa
出典データセット
uspto-grants-1998_03
特許番号
US05731125

関連ノート

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