Acrylamide → Acrylic acid n-decylacrylate acrylamide

HRID 1058495

反応式

HRID 1058495 の反応式
[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([O:16][C:17](=[O:20])[CH:18]=[CH2:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:21]([NH2:25])(=[O:24])[CH:22]=[CH2:23]>O1CCOCC1>[C:1]([OH:5])(=[O:4])[CH:2]=[CH2:3].[CH2:6]([O:16][C:17](=[O:20])[CH:18]=[CH2:19])[CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15].[C:21]([NH2:25])(=[O:24])[CH:22]=[CH2:23]

参加物

5

反応条件

温度
70 °C

実験手順

A solution was prepared of acrylic acid (10.0 g, 133 mmol), n-decylacrylate (3.0 g, 14.2 mmol) and acrylamide (3.0 g, 42.2 mmol) in dioxane (200 mL). After the solution was degassed with a rapid stream of nitrogen, AIBN (1.3 g) was added. The solution was degassed for a further thirty minutes and the reaction was then heated to 70° C. for 17 h. The polymer precipitated as a fibrous white solid as the reaction proceeded. The solution was cooled and the dioxane decanted. The residue was washed with ethyl acetate (600 mL) and the ethyl acetate was discarded. The polymer was finally washed with hexanes (300 mL) and dried in vacuo.

後処理

  1. customAfter the solution was degassed with a rapid stream of nitrogen, AIBN (1.3 g)
  2. additionwas added
  3. customThe solution was degassed for a further thirty minutes
  4. customThe polymer precipitated as a fibrous white solid as the reaction
  5. temperatureThe solution was cooled
  6. customthe dioxane decanted
  7. washThe residue was washed with ethyl acetate (600 mL)
  8. washThe polymer was finally washed with hexanes (300 mL)
  9. customdried in vacuo

出典と根拠

ORDレコード
ord-c7d61ca8b2c14dea9cd0edf3b8d7d5fb
出典データセット
uspto-grants-2003_02
特許番号
US06517826B1

関連ノート

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