Acrylamide → Acrylamide 2-Acrylamido-2-Methyl Propyl Sulfonic Acid

HRID 25920

反応式

HRID 25920 の反応式
[OH-].[Na+].[C:3]([NH:7][C:8]([CH3:15])([CH3:14])[CH2:9][S:10]([OH:13])(=[O:12])=[O:11])(=[O:6])[CH:4]=[CH2:5].C(N)(=O)C=C.CC(C(OOC(C)(C)C)=O)(C)C>O>[C:3]([NH2:7])(=[O:6])[CH:4]=[CH2:5].[C:3]([NH:7][C:8]([CH3:15])([CH3:14])[CH2:9][S:10]([OH:13])(=[O:11])=[O:12])(=[O:6])[CH:4]=[CH2:5]

参加物

6

反応物 4

HCID 6579AcrylamideHCID 14798Sodium HydroxideHCID 61238tert-BUTYL PEROXYPIVALATEHCID 653602-Acrylamido-2-methyl-1-propanesulfonic acid

生成物 1

HCID 86735510Acrylamide 2-Acrylamido-2-Methyl Propyl Sulfonic Acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Borax (0.6 g.) and 50% aqueous sodium hydroxide (7.2 g.) were dissolved in 52.4 g. of distilled water. 2-acrylamido-2-methyl propyl sulfonic acid (2-AMPSA) (20.4 g.) and acrylamide (AM) (39.4 g.) were dissolved in the caustic solution while maintaining the temperature at <20° C. by cooling. The pH of the final solution was adjusted to 8.0; the solution was then combined with Tween 85 (30.0 g.) and Mentor 28 (50.0 g.). The reaction was conducted according to the procedure of Example 31. 0.5 ml of a 0.01% FAS solution and 0.1 ml of Lupersol 11 was used; polymerization was maintained at <68° C. by cooling. The product was a stable emulsion (5000 cps viscosity).

後処理

  1. temperaturewhile maintaining the temperature at <20° C.
  2. temperatureby cooling
  3. custompolymerization
  4. temperaturewas maintained at <68° C.
  5. temperatureby cooling

出典と根拠

ORDレコード
ord-bcfc5a81563f4c31a349375bcebb3c0c
出典データセット
uspto-grants-1979_04
特許番号
US04147681

関連ノート

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