戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 359784作成日:2026年10月25日

Acrylamide → N-Hexadecylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate

https://huagongshe.com/reaction/359784

反応式

関与物質

役割名称HCID仕込み量
反応物AcrylamideHCID 6579—
反応物N-vinyl-2-pyrrolidoneHCID 6917—
反応物N-HexadecylacrylamideHCID 88828—
反応物Sodium Lauryl SulfateHCID 3423265—
反応物Sodium acrylamido-2-methyl-1-propyl sulfonateHCID 23669106—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒DimethylacetamideHCID 31374—
溶媒Aceton-methanolHCID 21894497—
生成物N-Hexadecylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonateHCID 131716743—

反応手順

A solution was prepared of 6.0 g of sodium dodecylsulfate in 300 mL of deoxygenated water. N-Hexadecylacrylamide, 0.666 g, was dissolved in this solution followed by 9.44 g of acrylamide, 8.92 g of DMA, 10.00 g of N-vinylpyrrolidinone (NVP) and 27.99 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 0.0518 g of 2,2'-azobis(N,N'-dimethylene-isobutyramidine) 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 blendor with methanol/acetone, filtered and dried under vacuum at 30 C. The yield of polymer was 42.21 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05003000
出典データセットuspto-grants-1991_03
ORD IDord-2ae7de8432c643b5b4fd18835008ff73
出典メモuspto-grants-1991_03