HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359782Generated: October 25, 2026
Acrylamide → N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone
https://huagongshe.com/reaction/359782
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acrylamide | HCID 6579 | — |
| Reactant | N-vinyl-2-pyrrolidone | HCID 6917 | — |
| Reactant | 2-Propenamide, N-octyl- | HCID 82370 | — |
| Reactant | Sodium Lauryl Sulfate | HCID 3423265 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Solvent | Aceton-methanol | HCID 21894497 | — |
| Product | N-1-Octylacrylamide Acrylamide DMA N-Vinylpyrrolidinone | HCID 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 followed by 18.30 g of acrylamide, 19.38 g of DMA and 21.73 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05003000 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-0bf9e01fad684d09bf85333167fbcf39 |
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| Source note | uspto-grants-1991_03 |
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