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HRID 358794作成日:2026年10月26日
Acrylamide → N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate
https://huagongshe.com/reaction/358794
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acrylamide | HCID 6579 | — |
| 反応物 | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| 反応物 | 2-Propenamide, N-octyl- | HCID 82370 | — |
| 反応物 | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| 反応物 | Sodium Lauryl Sulfate | HCID 3423265 | — |
| 反応物 | Sodium acrylamido-2-methyl-1-propyl sulfonate | HCID 23669106 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 溶媒 | Aceton-methanol | HCID 21894497 | — |
| 生成物 | N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate | HCID 131716742 | — |
反応手順
A solution was prepared of 6.0 g of sodium dodecylsulfate in 300 mL of deoxygenated water. N-1-octylacrylamide, 1.492 g, was dissolved in this solution followed by 13.98 g of acrylamide, 13.33 g of DMA, 14.94 g of N-vinylpyrrolidinone (NVP) and 41.81 g of sodium acrylamido-2-methylpropane sulfonate. The resulting solution was carefully transferred to a 1 L Morton style resin kettle fitted with a chilled water condenser, thermometer, inert gas sparger and mechanical stirrer. The temperature was adjusted to 25° C. and polymerization was initiated by the addition of 0.108 g of 2,2'-azobis(N,N,-dimethylene-isobutyramidine) 5z;- dihydrochloride. After stirring for 16 hr at 25'±0.2° C., a 250 mL portion of the viscous solution was added to 3 L of acetone. The precipitated polymer was then masticated in a Waring blender with methanol/acetone, filtered and dried under vacuum at 30° C. The yield of polymer was 110.04 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04997878 |
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| 出典データセット | uspto-grants-1991_03 |
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| ORD ID | ord-b698c6cdc11d405293b896ee0852ead3 |
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| 出典メモ | uspto-grants-1991_03 |
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