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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358793Generated: October 25, 2026

N-vinyl-2-pyrrolidone → N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone

https://huagongshe.com/reaction/358793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-vinyl-2-pyrrolidoneHCID 6917—
Reactant2-Propenamide, N-octyl-HCID 82370—
ReactantTetrafluoro-m-phenylenediamine dihydrochlorideHCID 149026—
ReactantSodium Lauryl SulfateHCID 3423265—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventAcrylamideHCID 6579—
SolventDimethylacetamideHCID 31374—
SolventAceton-methanolHCID 21894497—
ProductN-1-Octylacrylamide Acrylamide DMA N-VinylpyrrolidinoneHCID 131716804—

Reaction Steps

A solution was prepared of 3.0 g of sodium dodecylsulfate in 300 mL of deoxygenated water. N-1-octylacrylamide, 0.597 g, was dissolved in this solution folloW®d by 18.30 g of acrylamide, 19.38 g of DMA and 2I.73 g of N-vinylpyrrolidinone (NVP). 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 55.53 g. Other examples of these polymers are given in Table III.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997878
Source datasetuspto-grants-1991_03
ORD IDord-31efc3a66a4f4a569fa7ab4020729223
Source noteuspto-grants-1991_03