Methyl Isobutyl Ketone → 1-Ethoxy-2-(2-methoxyethoxy)ethane

HRID 1618836

反応式

HRID 1618836 の反応式
[C:1]([O:6][CH:7]([O:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)[CH3:8])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=[CH2:23])=[CH:20][CH:19]=1.C(C(C)=[O:31])C(C)C.N(C(C)(CC)C([O-])=O)=NC(C)(CC)C([O-])=O>CCCCCCC>[CH3:16][O:17][CH2:18][CH2:25][O:31][CH2:15][CH2:10][O:9][CH2:7][CH3:8].[C:1]([O:6][CH:7]([O:9][CH:10]1[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]1)[CH3:8])(=[O:5])[C:2]([CH3:4])=[CH2:3].[CH3:16][O:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=[CH2:23])=[CH:20][CH:19]=1

参加物

7

実験手順

A 500 ml three-necked flask was charged with 63.7 g (0.30 mol) of 1-cyclohexyloxyethyl methacrylate, 40.3 g (0.30 mol) of p-methoxystyrene and 300 ml of methyl isobutyl ketone. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) as a radical polymerization initiator was added to the mixture, and polymerization was performed in a nitrogen stream at 80° C. for six hours. The obtained reaction liquid was cooled, and poured in a large volume of heptane, thereby precipitating a polymer. The polymer crystal was collected by filtration, and dissolved in diethylene glycol ethyl methyl ether. The heptane and methyl isobutyl ketone contained in the solution were distilled off in vacuum, thereby obtaining a diethylene glycol ethyl methyl ether solution of polymer A1-6 (1-cyclohexyloxyethyl methacrylate/p-methoxystyrene).

後処理

  1. customThe obtained reaction liquid
  2. temperaturewas cooled
  3. customprecipitating a polymer
  4. filtrationThe polymer crystal was collected by filtration
  5. dissolutiondissolved in diethylene glycol ethyl methyl ether
  6. distillationwere distilled off in vacuum

出典と根拠

ORDレコード
ord-0c1dc38fc8a143e0a6949641ff9a707d
出典データセット
uspto-grants-2014_07
特許番号
US08771907B2

関連ノート

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