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HRID 358795作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/358795

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—

反応条件

温度0.20000000298023224 °C

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US04997878
出典データセットuspto-grants-1991_03
ORD IDord-83a3929c687e494bbf0aa26fff21d3ff
出典メモuspto-grants-1991_03