Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358794Generated: October 25, 2026

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

https://huagongshe.com/reaction/358794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylamideHCID 6579—
ReactantN-vinyl-2-pyrrolidoneHCID 6917—
Reactant2-Propenamide, N-octyl-HCID 82370—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
ReactantSodium Lauryl SulfateHCID 3423265—
ReactantSodium acrylamido-2-methyl-1-propyl sulfonateHCID 23669106—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
SolventAceton-methanolHCID 21894497—
ProductN-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone Sodium Acrylamido-2-methylpropane sulfonateHCID 131716742—

Reaction Conditions

Temperature0.20000000298023224 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997878
Source datasetuspto-grants-1991_03
ORD IDord-b698c6cdc11d405293b896ee0852ead3
Source noteuspto-grants-1991_03