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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359783생성일: 2026년 10월 25일

Acrylamide → N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonate

https://huagongshe.com/reaction/359783

반응식

참여 물질

역할이름HCID투입량
반응물AcrylamideHCID 6579—
반응물N-vinyl-2-pyrrolidoneHCID 6917—
반응물2-Propenamide, N-octyl-HCID 82370—
반응물Sodium Lauryl SulfateHCID 3423265—
반응물Sodium acrylamido-2-methyl-1-propyl sulfonateHCID 23669106—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매DimethylacetamideHCID 31374—
용매Aceton-methanolHCID 21894497—
생성물N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonateHCID 131716742—

반응 단계

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) 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05003000
출처 데이터셋uspto-grants-1991_03
ORD IDord-856992ccdffe4d9bb66445cc3cb1dd66
출처 메모uspto-grants-1991_03